Tobacco composition comprising a tobacco component and an aerosol forming material

ABSTRACT

A tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component and wherein the leaf tobacco material has a nicotine content of greater than 1.5% by weight of the leaf tobacco material and a method of making the tobacco composition. Also, an article comprising the tobacco composition for use in an aerosol provision system and a system comprising a device arranged to heat the tobacco composition and generate an aerosol from the tobacco composition.

The present application is a National Phase entry of PCT Application No. PCT/GB2020/050609, filed Mar. 11, 2020 which claims priority from GB Patent Application No. 1903287.9 filed Mar. 11, 2019, each of which is hereby fully incorporated herein by reference.

TECHNICAL FIELD

The present disclosure relates to a tobacco composition comprising an aerosol forming material, a method for manufacturing a tobacco composition and an article for use with an aerosol generation device, the article for use with the aerosol generation device comprising the tobacco composition.

BACKGROUND

Many tobacco industry products include an aerosolizable material, such as a tobacco composition. Articles, such as cigarettes, cigars and the like, burn the aerosolizable material during use to create tobacco smoke. Attempts have been made to provide alternatives to these types of articles, which burn the tobacco material, by creating products that release compounds without burning. Examples of such products are so-called heat-not-burn products, also known as tobacco heating products or tobacco heating devices, which release compounds by heating, but not burning, the aerosolizable material.

SUMMARY

In accordance with embodiments of the disclosure, in a first aspect there is provided a tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component and wherein the leaf tobacco material has a nicotine content of greater than 1.5% by weight of the leaf tobacco material.

In accordance with embodiments of the disclosure, in a second aspect there is provided a tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component, and wherein the leaf tobacco material comprises said aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material, and wherein the tobacco composition comprises said aerosol forming material in an amount between about 10% and about 30% by weight of the tobacco composition.

In accordance with embodiments of the disclosure, in a third aspect there is provided a tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component, and wherein the tobacco component comprises menthol in an amount of between about 3 mg and about 16 mg.

In accordance with embodiments of the disclosure, in a fourth aspect there is provided a method of manufacturing the tobacco composition of the first or second aspects above, the method comprising applying said aerosol forming material to said leaf tobacco material.

In accordance with embodiments of the disclosure, in a fifth aspect there is provided a tobacco composition manufactured using the method of the fourth aspect above.

In accordance with embodiments of the disclosure, in a sixth aspect there is provided a use of a tobacco composition according to the first, second, third or fourth aspects above in an article for use within an aerosol delivery system.

In accordance with embodiments of the disclosure, in a seventh aspect there is provided an article for use in an aerosol provision system comprising the tobacco composition as set out in the first, second, third and fourth aspects above.

In accordance with embodiments of the disclosure, in an eighth aspect there is provided a system comprising a tobacco composition as set out in the first, second, third and fourth aspects above and a device arranged to heat the tobacco composition and generate an aerosol from the tobacco composition.

BRIEF DESCRIPTION OF THE DRAWINGS

Embodiments of the disclosure will now be described, by way of example only, with reference to the accompanying drawings, in which:

FIG. 1 shows a flowchart for a process for making paper reconstituted tobacco;

FIG. 2 shows a flowchart for a process for making extruded tobacco;

FIG. 3 shows a flowchart for a process for making a tobacco composition:

FIG. 4 is a side-on cross-sectional view of an article for use with a non-combustible aerosol provision device, the article including a mouthpiece;

FIG. 5a is a side-on cross sectional view of a further article for use with a non-combustible aerosol provision device, in this example the article including a capsule-containing mouthpiece;

FIG. 5b is a cross sectional view of the capsule-containing mouthpiece shown in FIG. 5 a:

FIG. 6 is a perspective illustration of a non-combustible aerosol provision device for generating aerosol from the aerosol generating material of the articles of FIGS. 4, 5 a and 5 b:

FIG. 7 illustrates the device of FIG. 6 with the outer cover removed and without an article present:

FIG. 8 is a side view of the device of FIG. 6 in partial cross-section;

FIG. 9 is an exploded view of the device of FIG. 6, with the outer cover omitted;

FIG. 10A is a cross sectional view of a portion of the device of FIG. 6;

FIG. 10B is a close-up illustration of a region of the device of FIG. 6; and

FIG. 11 is a flow diagram illustrating a method of manufacturing an article for use with a non-combustible aerosol provision device.

DETAILED DESCRIPTION

As used herein, the term “delivery system” is intended to encompass systems that deliver a substance to a user, and includes:

-   -   non-combustible aerosol provision systems that release compounds         from an aerosolizable material without combusting the         aerosolizable material, such as electronic cigarettes, tobacco         heating products, and hybrid systems to generate aerosol using a         combination of aerosolizable materials;     -   articles comprising aerosolizable material and configured to be         used within one of these non-combustible aerosol provision         systems; and     -   aerosol-free delivery systems, such as lozenges, gums, patches,         articles comprising inhalable powders, and smokeless tobacco         products such as snus and snuff, which deliver a material to a         user without forming an aerosol.

According to the present disclosure, a “non-combustible” aerosol provision system is one where a constituent aerosolizable material of the aerosol provision system (or component thereof) is not combusted or burned in order to facilitate delivery to a user. The non-combustible aerosol provision system

In one embodiment, the delivery system is a non-combustible aerosol provision system, such as a powered non-combustible aerosol provision system.

In one embodiment, the non-combustible aerosol provision system is an electronic cigarette, also known as a vaping device or electronic nicotine delivery system (END).

In one embodiment, the non-combustible aerosol provision system is a tobacco heating system, also known as a heat-not-burn system.

In one embodiment, the non-combustible aerosol provision system is a hybrid system to generate aerosol using a combination of aerosolizable materials, one or a plurality of which may be heated. Each of the aerosolizable materials may be, for example, in the form of a solid, liquid or gel. In one embodiment, the hybrid system comprises a liquid or gel aerosolizable material and a solid aerosolizable material. The solid aerosolizable material may comprise, for example, tobacco material or a non-tobacco product.

Typically, the non-combustible aerosol provision system may comprise a non-combustible aerosol provision device, also referred to herein as an aerosol generation device, and an article for use with the non-combustible aerosol provision system. However, it is envisaged that articles which themselves comprise a means for powering an aerosol generating component may themselves form the non-combustible aerosol provision system.

In one embodiment, the non-combustible aerosol provision device may comprise a power source and a controller. The power source may be an electric power source or an exothermic power source. In one embodiment, the exothermic power source comprises a carbon substrate which may be energized so as to distribute power in the form of heat to an aerosolizable material or heat transfer material in proximity to the exothermic power source. In one embodiment, the power source, such as an exothermic power source, is provided in the article so as to form the non-combustible aerosol provision.

In one embodiment, the article for use with the non-combustible aerosol provision device may comprise an aerosolizable material, an aerosol generating component, an aerosol generating area, a mouthpiece, and/or an area for receiving aerosolizable material.

In one embodiment, the aerosol generating component is a heater capable of interacting with the aerosolizable material so as to release one or more volatiles from the aerosolizable material to form an aerosol. In one embodiment, the aerosol generating component is capable of generating an aerosol from the aerosolizable material without heating. For example, the aerosol generating component may be capable of generating an aerosol from the aerosolizable material without applying heat thereto, for example via one or more of vibrational, mechanical, pressurization or electrostatic means.

In one embodiment, the aerosolizable material may comprise an active material, an aerosol forming material and optionally one or more functional materials. The active material may comprise nicotine (optionally contained in tobacco or a tobacco derivative) or one or more other non-olfactory physiologically active materials. A non-olfactory physiologically active material is a material which is included in the aerosolizable material in order to achieve a physiological response other than olfactory perception.

The aerosol forming material may comprise one or more of glycerine, glycerol, propylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,3-butylene glycol, erythritol, meso-Erythritol, ethyl vanillate, ethyl laurate, a diethyl suberate, triethyl citrate, triacetin, a diacetin mixture, benzyl benzoate, benzyl phenyl acetate, tributyrin, lauryl acetate, lauric acid, myristic acid, and propylene carbonate.

The one or more functional materials may comprise one or more of flavors, carriers, pH regulators, stabilizers, and/or antioxidants.

In one embodiment, the article for use with the non-combustible aerosol provision device may comprise aerosolizable material or an area for receiving aerosolizable material. In one embodiment, the article for use with the non-combustible aerosol provision device may comprise a mouthpiece. The area for receiving aerosolizable material may be a storage area for storing aerosolizable material. For example, the storage area may be a reservoir. In one embodiment, the area for receiving aerosolizable material may be separate from, or combined with, an aerosol generating area.

Aerosolizable material, which also may be referred to herein as aerosol generating material and aerosol generating substrate, is material that is capable of generating aerosol, for example when heated, irradiated or energized in any other way. Aerosolizable material may, for example, be in the form of a solid, liquid or gel which may or may not contain nicotine and/or flavorants. In some embodiments, the aerosolizable material may comprise an “amorphous solid”, which may alternatively be referred to as a “monolithic solid” (i.e. non-fibrous). In some embodiments, the amorphous solid may be a dried gel. The amorphous solid is a solid material that may retain some fluid, such as liquid, within it. In some embodiments, the aerosolizable material may for example comprise from about 50 wt %, 60 wt % or 70 wt % of amorphous solid, to about 90 wt %, 95 wt % or 100 wt % of amorphous solid.

The aerosolizable material may be present on a substrate. The substrate may, for example, be or comprise paper, card, paperboard, cardboard, reconstituted aerosolizable material, a plastics material, a ceramic material, a composite material, glass, a metal, or a metal alloy.

An aerosol modifying agent is a substance that is able to modify aerosol in use. The agent may modify aerosol in such a way as to create a physiological or sensory effect on the human body. Example aerosol modifying agents are flavorants and sensates. A sensate creates an organoleptic sensation that can be perceived through the senses, such as a cool or sour sensation.

A susceptor is material that is heatable by penetration with a varying magnetic field, such as an alternating magnetic field. The heating material may be an electrically-conductive material, so that penetration thereof with a varying magnetic field causes induction heating of the heating material. The heating material may be magnetic material, so that penetration thereof with a varying magnetic field causes magnetic hysteresis heating of the heating material. The heating material may be both electrically-conductive and magnetic, so that the heating material is heatable by both heating mechanisms.

Induction heating is a process in which an electrically-conductive object is heated by penetrating the object with a varying magnetic field. The process is described by Faraday's law of induction and Ohm's law. An induction heater may comprise an electromagnet and a device for passing a varying electrical current, such as an alternating current, through the electromagnet. When the electromagnet and the object to be heated are suitably relatively positioned so that the resultant varying magnetic field produced by the electromagnet penetrates the object, one or more eddy currents are generated inside the object. The object has a resistance to the flow of electrical currents. Therefore, when such eddy currents are generated in the object, their flow against the electrical resistance of the object causes the object to be heated. This process is called Joule, ohmic, or resistive heating. An object that is capable of being inductively heated is known as a susceptor.

In one embodiment, the susceptor is in the form of a closed circuit. It has been found that, when the susceptor is in the form of a closed circuit, magnetic coupling between the susceptor and the electromagnet in use is enhanced, which results in greater or improved Joule heating.

Magnetic hysteresis heating is a process in which an object made of a magnetic material is heated by penetrating the object with a varying magnetic field. A magnetic material can be considered to comprise many atomic-scale magnets, or magnetic dipoles. When a magnetic field penetrates such material, the magnetic dipoles align with the magnetic field. Therefore, when a varying magnetic field, such as an alternating magnetic field, for example as produced by an electromagnet, penetrates the magnetic material, the orientation of the magnetic dipoles changes with the varying applied magnetic field. Such magnetic dipole reorientation causes heat to be generated in the magnetic material.

When an object is both electrically-conductive and magnetic, penetrating the object with a varying magnetic field can cause both Joule heating and magnetic hysteresis heating in the object. Moreover, the use of magnetic material can strengthen the magnetic field, which can intensify the Joule heating.

In each of the above processes, as heat is generated inside the object itself, rather than by an external heat source by heat conduction, a rapid temperature rise in the object and more uniform heat distribution can be achieved, particularly through selection of suitable object material and geometry, and suitable varying magnetic field magnitude and orientation relative to the object. Moreover, as induction heating and magnetic hysteresis heating do not require a physical connection to be provided between the source of the varying magnetic field and the object, design freedom and control over the heating profile may be greater, and cost may be lower.

Articles, for instance those in the shape of rods, are often named according to the product length: “regular” (typically in the range 68-75 mm, e.g. from about 68 mm to about 72 mm), “short” or “mini” (68 mm or less), “king-size” (typically in the range 75-91 mm, e.g. from about 79 mm to about 88 mm), “long” or “super-king” (typically in the range 91-105 mm, e.g. from about 94 mm to about 101 mm) and “ultra-long” (typically in the range from about 110 mm to about 121 mm).

They are also named according to the product circumference: “regular” (about 23-25 mm), “wide” (greater than 25 mm), “slim” (about 22-23 mm), “demi-slim” (about 19-22 mm), “super-slim” (about 16-19 mm), and “micro-slim” (less than about 16 mm).

Accordingly, an article in a king-size, super-slim format will, for example, have a length of about 83 mm and a circumference of about 17 mm.

Each format may be produced with mouthpieces of different lengths. The mouthpiece length will be from about 30 mm to 50 mm. A tipping paper connects the mouthpiece to the aerosol generating material and will usually have a greater length than the mouthpiece, for example from 3 to 10 mm longer, such that the tipping paper covers the mouthpiece and overlaps the aerosol generating material, for instance in the form of a rod of substrate material, to connect the mouthpiece to the rod.

Articles and their aerosol generating materials and mouthpieces described herein can be made in, but are not limited to, any of the above formats.

The terms ‘upstream’ and ‘downstream’ used herein are relative terms defined in relation to the direction of mainstream aerosol drawn though an article or device in use.

The filamentary tow material described herein can comprise cellulose acetate fiber tow. The filamentary tow can also be formed using other materials used to form fibers, such as polyvinyl alcohol (PVOH), polylactic acid (PLA), polycaprolactone (PCL), poly(1-4 butanediol succinate) (PBS), poly(butylene adipate-co-terephthalate)(PBAT), starch based materials, cotton, aliphatic polyester materials and polysaccharide polymers or a combination thereof. The filamentary tow may be plasticized with a suitable plasticizer for the tow, such as triacetin where the material is cellulose acetate tow, or the tow may be non-plasticized. The tow can have any suitable specification, such as fibers having a ‘Y’ shaped or other cross section such as ‘X’ shaped, filamentary denier values between 2.5 and 15 denier per filament, for example between 8.0 and 11.0 denier per filament and total denier values of 5,000 to 50,000, for example between 10,000 and 40,000.

As used herein, the term “tobacco material” refers to any material comprising tobacco or derivatives or substitutes thereof. The term “tobacco material” may include one or more of tobacco, tobacco derivatives, expanded tobacco, reconstituted tobacco or tobacco substitutes. The tobacco material may comprise one or more of ground tobacco, tobacco fiber, cut tobacco, extruded tobacco, leaf tobacco, tobacco stem, reconstituted tobacco and/or tobacco extract. As used herein, “leaf tobacco” means cut lamina tobacco.

As used herein, the terms “flavor” and “flavorant” refer to materials which, where local regulations permit, may be used to create a desired taste or aroma in a product for adult consumers.

As used herein, the terms “flavor” and “flavorant” refer to materials which, where local regulations permit, may be used to create a desired taste or aroma in a product for adult consumers. They may include extracts (e.g., licorice, hydrangea. Japanese white bark magnolia leaf, chamomile, fenugreek, clove, menthol, Japanese mint, aniseed, cinnamon, herb, wintergreen, cherry, berry, peach, apple, Drambuie, bourbon, scotch, whiskey, spearmint, peppermint, lavender, cardamom, celery, cascarilla, nutmeg, sandalwood, bergamot, geranium, honey essence, rose oil, vanilla, lemon oil, orange oil, cassia, caraway, cognac, jasmine, ylang-ylang, sage, fennel, piment, ginger, anise, coriander, coffee, or a mint oil from any species of the genus Mentha), flavor enhancers, bitterness receptor site blockers, sensorial receptor site activators or stimulators, sugars and/or sugar substitutes (e.g., sucralose, acesulfame potassium, aspartame, saccharine, cyclamates, lactose, sucrose, glucose, fructose, sorbitol, or mannitol), and other additives such as charcoal, chlorophyll, minerals, botanicals, or breath freshening agents. They may be imitation, synthetic or natural ingredients or blends thereof. They may be in any suitable form, for example, oil, liquid, or powder.

Preferably the aerosol generating material or substrate 3 is formed from tobacco material as described herein, which includes a tobacco component. The tobacco component comprises leaf tobacco. In some embodiments, the tobacco component comprises tobacco material selected from the group consisting of: extruded tobacco, bandcast tobacco, and mixtures thereof.

The leaf tobacco which may be used in the tobacco compositions described herein may be any suitable tobacco, such as single grades or blends, cut rag or whole leaf, including Virginia (flue-cured and/or air cured) and/or Burley and/or Oriental. The tobacco composition may comprise a mixture of any of these leaf tobacco materials.

The leaf tobacco is present in an amount of between about 10% and about 90% by weight of the tobacco component. In some embodiments, the leaf tobacco may be present in an amount of between of between about 11% and about 48%, about 12% and about 46%, about 13% and about 44%, about 14% and about 42%, about 15% and about 40%, about 16% and about 38%, about 17% and about 36%, about 18% and about 34% or about 19% and about 32% by weight of the tobacco component. In a preferred embodiment, the tobacco component comprises leaf tobacco in an amount of between about 15% and about 25% by weight of the tobacco component, between about 35% and about 45% or between about 55% and 65%. In preferred embodiments, the tobacco component may comprise leaf tobacco in an amount of about 15%, about 16%, about 17%, about 18%, about 19%, about 20%, about 21%, about 22%, about 23%, about 24%, about 25%, about 26%, about 27%, about 28%, about 29% or about 30% by weight of the tobacco component.

In some embodiments, the tobacco component comprises leaf tobacco in an amount of about 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49% or 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69% or 70%.

In the compositions described herein, where amounts are given in % by weight, for the avoidance of doubt this refers to a dry weight basis, unless specifically indicated to the contrary. Thus, any water that may be present in the tobacco composition, or in any component thereof, is entirely disregarded for the purposes of the determination of the weight %. The water content of the tobacco compositions described herein may vary and may be, for example, from 5 to 15% by weight. The water content of the tobacco compositions described herein may vary according to, for example, the temperature, pressure and humidity conditions at which the compositions are maintained. The water content can be determined by Karl-Fisher analysis, as described herein.

On the other hand, for the avoidance of doubt, even when the aerosol forming material is a component that is in liquid phase, such as glycerol or propylene glycol, any component other than water is included in the weight of the tobacco composition. However, when the aerosol forming material is provided in the tobacco component of the tobacco composition, or in the filler component (if present) of the tobacco composition, instead of or in addition to being added separately to the tobacco composition, the aerosol forming material is not included in the weight of the tobacco component or filler component, but is included in the weight of the “aerosol forming material” in the weight % as defined herein. All other ingredients present in the tobacco component are included in the weight of the tobacco component, even if of non-tobacco origin (for example non-tobacco fibers in the case of paper reconstituted tobacco).

The tobacco components described herein contain nicotine. The nicotine content is from 0.5 to 2% by weight of the tobacco component, and may be, for example, from 0.5 to 1.75% by weight of the tobacco component, from 0.8 to 1.2% by weight of the tobacco component or from about 0.8 to about 1.75% by weight of the tobacco component. In embodiments, the nicotine content may be from 0.8 to 1.0% by weight of the tobacco component.

According to embodiments of one aspect of the disclosure, there is provided a tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco in an amount of between about 10% and about 90% by weight of the tobacco component and wherein the leaf tobacco has a nicotine content of greater than 1.5% by weight of the leaf tobacco.

It may be important to control the nicotine content of the composition. In conventional tobacco heating products, the tobacco composition mainly comprises reconstituted tobacco material. The nicotine content of reconstituted tobacco material is generally relatively low. For example, the reconstituted tobacco material may comprise nicotine in an amount of less than about 1.5% by weight of the reconstituted tobacco material. Increasing the nicotine content of such compositions is challenging.

The inventors have found that the nicotine content of the tobacco composition may be carefully controlled by incorporating leaf tobacco into the composition, in addition to the reconstituted tobacco material. In particular, incorporating leaf tobacco having a nicotine content of more than 1.5% (by weight of the composition) into the composition has been found to be particularly advantageous. Incorporating leaf tobacco having a nicotine content of greater than about 1.5% by weight has been found to enhance the organoleptic properties (e.g. taste) of the tobacco composition when heated.

Without wishing to be bound by theory, it is thought that incorporating leaf tobacco material having a nicotine content of greater than 1.5% by weight of the leaf tobacco material into the composition facilitates the release of components from the tobacco composition that have a positive impact on the sensory properties of the tobacco composition when it is heated by an aerosol generation device. Advantageously, the amount of nicotine delivered to a user from the tobacco composition comprising leaf tobacco material having a nicotine content of greater than 1.5% by weight of the leaf tobacco material when it is heated in an aerosol generation device may be similar to the amount of nicotine delivered to a user of a conventional combustible smoking article.

In an embodiment, the tobacco material consists essentially of the tobacco component as defined herein and the aerosol forming material as defined herein. In an embodiment, the tobacco material consists of the tobacco component as defined herein and the aerosol forming material as defined herein.

The tobacco composition comprises a tobacco component and an aerosol forming material. The tobacco component may comprise leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component and the leaf tobacco material may comprise said aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material. The tobacco composition may comprise said aerosol forming material in an amount between about 10% and about 30% by weight of the tobacco composition. Preferably, the tobacco composition comprises the aerosol forming material in an amount of between about 10% and about 20% by weight of the tobacco composition.

The inclusion of aerosol forming material in an amount of between about 10% and about 30% by weight of the tobacco composition has been found to further enhance the sensory properties of the tobacco composition when heated by an aerosol generation device. Advantageously, the loading of the aerosol generating material of between about 10% and about 30% by weight of the tobacco composition may render the sensory properties of the composition similar to the sensory properties of a conventional combustible smoking article.

The tobacco composition may comprise a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component, and wherein the tobacco component comprises menthol in an amount of between about 3 mg to about 16 mg. Advantageously, the loading of the menthol in an amount of between about 3 mg and about 16 mg by weight of the tobacco component may improve the sensory properties of the tobacco composition when it is heated by an aerosol generation device.

The leaf tobacco has a nicotine content of greater than 1.5% by weight of the leaf tobacco. In some embodiments, the leaf tobacco has a nicotine content of between 1.5% and about 5% by weight of the leaf tobacco, preferably between about 1.5% and about 4% by weight of the leaf tobacco. The leaf tobacco may have a nicotine content of 1.5%, 1.6%, 1.7%, 1.8%, 1.9%, 2%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8%, 2.9%, 3%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9% or 5% by weight of the leaf tobacco. In some embodiments, the leaf tobacco has a nicotine content of more than about 1.5% and up to about 4% by weight of the leaf tobacco material.

The remainder of the tobacco component may comprise paper reconstituted tobacco, extruded tobacco, bandcast reconstituted tobacco, or a combination of bandcast reconstituted tobacco and another form of tobacco, such as tobacco granules. Preferably, the tobacco component comprises paper reconstituted tobacco material.

Paper reconstituted tobacco refers to tobacco material formed by a process in which tobacco feedstock is extracted with a solvent to afford an extract of solubles and a residue comprising fibrous material, and then the extract (usually after concentration, and optionally after further processing) is recombined with fibrous material from the residue (usually after refining of the fibrous material, and optionally with the addition of a portion of non-tobacco fibers) by deposition of the extract onto the fibrous material. The process of recombination resembles the process for making paper.

The paper reconstituted tobacco may be any type of paper reconstituted tobacco that is known in the art. In a particular embodiment, the paper reconstituted tobacco is made from a feedstock comprising one or more of tobacco strips, tobacco stems, and whole leaf tobacco. In a further embodiment, the paper reconstituted tobacco is made from a feedstock consisting of tobacco strips and/or whole leaf tobacco, and tobacco stems. However, in other embodiments, scraps, fines and winnowings can alternatively or additionally be employed in the feedstock.

The paper reconstituted tobacco for use in the tobacco material described herein may be prepared by methods which are known to those skilled in the art for preparing paper reconstituted tobacco.

Referring to FIG. 1, tobacco furnish such as leaf, strips, stems, scraps, fines, and/or winnowings (in some embodiments, leaf, strips and stems), are initially mixed with an aqueous solvent (e.g. water, water and water miscible solvents such as ethanol). Distilled water, deionized water, or tap water may be employed. The suspension of tobacco in the solvent is agitated by stirring or shaking for instance in order to increase the rate of extraction of the soluble portion from the fibrous portion of tobacco. The agitation is typically carried out for half an hour up to 6 hours. Agitation may be achieved in an agitator that comprises a vessel and a blade to achieve agitation. The amount of solvent in the suspension can vary widely from about 75 to 99% by weight of the suspension, depending on the tobacco furnish, the type of solvent and agitation equipment (in particular the blade type), and the temperature of the suspension. The typical range of suspension temperature is about 10° C. to about 100° C.

The soluble portion of the tobacco furnish is separated from the insoluble fibrous portion of tobacco, for example by pressing with a pneumatic, hydraulic or mechanical press, or by filtration. After the separation, the fibrous portion of tobacco is typically subjected to mechanical refining to produce a fibrous pulp. Suitable refiners can be typically disc refiners or conical refiners. The fibrous pulp will be then formed into a base web comprising the tobacco fibrous pulp on a papermaking station, such as a Fourdrinier type papermaking machine. It is typically laid onto a flat wire belt where excess water is removed by gravity drain and suction drain. Non-tobacco fiber, such as cellulose, wheat fiber or wood fiber, may be included with the tobacco-derived fibrous portion at this stage. The soluble portion of the tobacco feedstock is concentrated using any known type of concentrator such as film evaporator or vacuum evaporator. After concentration, ingredients such as aerosol forming materials (as defined herein), casings, for example cocoa, liquorice, and acids such as malic acid, or flavors (as defined herein) may be added and mixed with the concentrated tobacco solubles. Then concentrated tobacco solubles potentially containing aerosol forming materials and/or casings and/or flavors are recombined with the dried tobacco fibrous sheet to form reconstituted tobacco. The concentrated solubles can be added back to the fibrous web with various methods, such as spraying, coating, saturating, sizing.

Finally, the reconstituted tobacco is dried. It may optionally be cut into strips or wound into a roll and then slit into bobbins or shredded into cut rag. As used herein, the terms “flavor” and “flavoring” refer to materials which, where local regulations permit, may be used to create a desired taste or aroma in a product for adult consumers. They may include extracts (e.g., liquorice, hydrangea, Japanese white bark magnolia leaf, chamomile, fenugreek, clove, menthol, Japanese mint, aniseed, cinnamon, herb, wintergreen, cherry, berry, peach, apple, Drambuie, bourbon, scotch, whiskey, spearmint, peppermint, lavender, cardamom, celery, cascarilla, nutmeg, sandalwood, bergamot, geranium, honey essence, rose oil, vanilla, lemon oil, orange oil, cassia, caraway, cognac, jasmine, ylang-ylang, sage, fennel, piment, ginger, anise, coriander, coffee, or a mint oil from any species of the genus Mentha), flavor enhancers, bitterness receptor site blockers, sensorial receptor site activators or stimulators, sugars and/or sugar substitutes (e.g., sucralose, acesulfame potassium, aspartame, saccharine, cyclamates, lactose, sucrose, glucose, fructose, sorbitol, or mannitol), and other additives such as charcoal, chlorophyll, minerals, botanicals, or breath freshening agents. They may be imitation, synthetic or natural ingredients or blends thereof. They may be in any suitable form, for example, oil, liquid, or powder. Examples of paper reconstituted tobacco that may be used in the present disclosure are provided in the Examples.

The tobacco component may comprise a mixture of leaf tobacco and paper reconstituted tobacco material. The paper reconstituted tobacco material may have a nicotine content of less than the nicotine content of an equivalent weight of the leaf tobacco. For example, the reconstituted tobacco material may have a nicotine content of less than 1.5% by weight of the reconstituted tobacco material.

It has been advantageously found that using a tobacco leaf with nicotine content higher than 1.5% in combination with a lower nicotine base material, such as paper reconstituted tobacco, provides a tobacco material with an appropriate nicotine level but better sensory performance than the use of paper reconstituted tobacco alone.

The tobacco component may comprise paper reconstituted tobacco in an amount of between about 10% to about 90% by weight of the tobacco component. In embodiments, the paper reconstituted tobacco is present in an amount of from 10% to 80% by weight or 20% to 70% by weight, of the tobacco component. In some embodiments, the tobacco component comprises paper reconstituted tobacco material in an amount of between about 50% and about 90% of the tobacco component.

In some embodiments, the reconstituted tobacco may be present in an amount of between of between about 10% and about 89%, about 20% and about 88%, about 30% and about 87%, about 40% and about 86%, about 50% and about 85%, about 60% and about 84%, about 70% and about 83% by weight of the tobacco component. In some embodiments, the tobacco component may comprise reconstituted tobacco in an amount of between about 75% and about 85% by weight of the tobacco component.

In preferred embodiments, the tobacco component may comprise reconstituted tobacco in an amount of about 70%, about 71%, about 72%, about 73%, about 74%, about 75%, about 76%, about 77%, about 78%, about 79%, about 80%, about 81%, about 82%, about 83%, about 84% or about 85% by weight of the tobacco component.

In one embodiment, the leaf tobacco is present in an amount of at least 10% by weight of the tobacco component, while the remainder of the tobacco component comprises paper reconstituted tobacco, bandcast reconstituted tobacco, or a combination of bandcast reconstituted tobacco and another form of tobacco such as tobacco granules.

The reconstituted tobacco material may have a density of less than about 700 milligrams per cubic centimeter (mg/cc).

Such tobacco material has been found to be particularly effective at providing an aerosol generating material which can be heated quickly to release an aerosol, as compared to denser materials. For instance, the inventors tested the properties of various aerosol generating materials, such as bandcast reconstituted tobacco material and paper reconstituted tobacco material, when heated. It was found that, for each given aerosol generating material, there is a particular zero heat flow temperature below which net heat flow is endothermic, in other words more heat enters the material than leaves the material, and above which net heat flow is exothermic, in other words more heat leaves the material than enters the material, while heat is applied to the material. Materials having a density less than 700 mg/cc had a lower zero heat flow temperature. Since a significant portion of the heat flow out of the material is via the formation of aerosol, having a lower zero heat flow temperature has a beneficial effect on the time it takes to first release aerosol from the aerosol generating material. For instance, aerosol generating materials having a density of less than 700 mg/cc were found to have a zero heat flow temperature of less than 164° C., as compared to materials with a density over 700 mg/cc, which had zero heat flow temperatures greater than 164° C. The density of the aerosol generating material also has an impact on the speed at which heat conducts through the material, with lower densities, for instance those below 700 mg/cc, conducting heat more slowly through the material, and therefore enabling a more sustained release of aerosol.

The weight ratio of the leaf tobacco relative to the paper reconstituted tobacco material may be 10:90, 11:89, 12:88, 13:87, 14:86, 15:85, 16:84, 17:83, 18:82, 19:81, 20:80, 21:79, 22:78, 23:77, 24:76, 25:75, 26:74, 27:73, 28:72, 29:71, 30:70, 31:69, 32:68, 33:67, 34:66, 35:65, 36:64, 37:63, 38:62, 39:61, 40:60, 41:59, 42:58, 43:57, 44:56, 45:55, 46:54, 47:53, 48:52, 49:51, 50:50, 51:49, 52:48, 53:47, 54:46, 55:45, 56:44, 57:43, 58:42, 59:41, 60:40, 61:39, 62:38, 63:37, 64:36, 65:35, 66:34, 67:33, 68:32, 69:31, 70:30, 71:29, 72:28, 73:27, 74:26, 75:25, 76:24, 77:23, 78:22, 79:21, 80:20, 81:19, 82:18, 83:17, 84:16, 85:15, 86:14, 87:13, 88:12, 89:11 or 90:10 (weight of leaf tobacco:weight paper reconstituted tobacco).

Preferably, the aerosol generating material 3 comprises reconstituted tobacco material having a density of less than about 700 mg/cc, for instance paper reconstituted tobacco material. More preferably, the aerosol generating material 3 comprises reconstituted tobacco material having a density of less than about 600 mg/cc. Alternatively or in addition, the aerosol generating material 3 preferably comprises reconstituted tobacco material having a density of at least 350 mg/cc, which is considered to allow for a sufficient amount of heat conduction through the material.

The tobacco composition comprises an aerosol forming material. In this context, an “aerosol forming material” is an agent that promotes the generation of an aerosol. An aerosol forming material may promote the generation of an aerosol by promoting an initial vaporization and/or the condensation of a gas to an inhalable solid and/or liquid aerosol. In some embodiments, an aerosol forming material may improve the delivery of flavor from the aerosol generating material.

In general, any suitable aerosol forming material or agents may be included in the aerosol generating material of the disclosure. Suitable aerosol forming materials include, but are not limited to: a polyol such as sorbitol, glycerol, and glycols like propylene glycol or triethylene glycol; a non-polyol such as monohydric alcohols, high boiling point hydrocarbons, acids such as lactic acid, glycerol derivatives, esters such as diacetin, triacetin, triethylene glycol diacetate, triethyl citrate or myristates including ethyl myristate and isopropyl myristate and aliphatic carboxylic acid esters such as methyl stearate, dimethyl dodecanedioate and dimethyl tetradecanedioate.

In a preferred embodiment, the aerosol forming material is selected from the group consisting of: glycerol, sorbitol, propylene glycol, triethylene glycol, lactic acid, diacetin, triacetin, triethylene glycol diacetate, triethyl citrate, ethyl myristate, isopropyl myristate, methyl stearate, dimethyl dodecanedioate, dimethyl tetradecanedioate, and mixtures thereof.

The aerosol forming material has been found to improve the sensory performance of a an article for use with an aerosol generation device comprising the tobacco composition, by helping to transfer compounds such as flavor compounds from the tobacco material to the consumer.

The aerosol forming material may be included in any component of the tobacco composition. Alternatively or additionally the aerosol forming material may be added to the tobacco composition separately. In either case, the total amount of the aerosol forming material in the tobacco material should be as defined herein.

The leaf tobacco material may comprise the aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material. In other embodiments, the leaf tobacco may comprise the aerosol forming material in an amount of up to about 20% or between about 15% and about 20% by weight of the leaf tobacco. The leaf tobacco may comprise the aerosol forming material in an amount of from about 5%, about 10% or about 15% by weight of the leaf tobacco.

To achieve an overall level of aerosol forming material between 10% and 20% by weight of the tobacco material, it has been advantageously found that this can be added in higher weight percentages to the another component of the tobacco material, such as reconstituted tobacco material.

According to embodiments of one aspect of the disclosure, a tobacco composition is provided comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component, and wherein the leaf tobacco material comprises said aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material, and wherein the tobacco composition comprises said aerosol forming material in an amount between about 10% and about 30% by weight of the tobacco composition. Preferably, the tobacco composition comprises the aerosol forming material in an amount of between about 10% and about 20% by weight of the tobacco composition.

In some embodiments, the aerosol forming material may be glycerol, propylene glycol, or a mixture of glycerol and propylene glycol. Preferably, the aerosol forming material comprises glycerol. Glycerol may be present in an amount of from 10 to 20% by weight of the tobacco material, for example 13 to 16% by weight of the composition, or about 14% or 15% by weight of the composition. Propylene glycol, if present, may be present in an amount of from 0.1 to 0.3% by weight of the composition.

The aerosol forming material may be included in a component of the tobacco composition. For example, the aerosol forming material may be included in the reconstituted tobacco and/or in a filler component, if present.

Alternatively or additionally the aerosol forming material may be applied to the tobacco material separately. In either case, the total amount of the aerosol forming material in the tobacco material should be as defined herein.

The paper reconstituted tobacco material may comprise the aerosol forming material. The paper reconstituted tobacco material may comprise the aerosol forming material in an amount of between about 10% and about 20% by weight of the reconstituted tobacco material. In some embodiments, the paper reconstituted tobacco material may comprise the aerosol forming material in an amount of about 10%, about 11%, about 12%, about 13%, about 14%, about 15%, about 16%, about 17%, about 18%, about 19% or about 20% by weight of the reconstituted tobacco material.

The tobacco material described herein can contain an aerosol modifying agent, such as any of the flavors described herein. In one embodiment, the tobacco material contains menthol, forming a mentholated article. The tobacco material can comprise from 3 mg to 20 mg of menthol, preferably between 5 mg and 18 mg and more preferably between 8 mg and 16 mg of menthol. In the present example, the tobacco material comprises 16 mg of menthol. The tobacco material can contain between 2% and 8% by weight of menthol, preferably between 3% and 7% by weight of menthol and more preferably between 4% and 5.5% by weight of menthol. In one embodiment, the tobacco material includes 4.7% by weight of menthol. Such high levels of menthol loading can be achieved using a high percentage of reconstituted tobacco material, for instance greater than 50% of the tobacco material by weight. Alternatively or additionally, the use of a high volume of aerosol generating material, for instance tobacco material, can increase the level of menthol loading that can be achieved, for instance where greater than about 500 mm3 or suitably more than about 1000 mm3 of aerosol generating material, such as tobacco material, are used.

The tobacco material may be provided in the form of cut rag tobacco. The cut rag tobacco can have a cut width of at least 15 cuts per inch (about 5.9 cuts per cm, equivalent to a cut width of about 1.7 mm). Preferably, the cut rag tobacco has a cut width of at least 18 cuts per inch (about 7.1 cuts per cm, equivalent to a cut width of about 1.4 mm), more preferably at least 20 cuts per inch (about 7.9 cuts per cm, equivalent to a cut width of about 1.27 mm). In one example, the cut rag tobacco has a cut width of 22 cuts per inch (about 8.7 cuts per cm, equivalent to a cut width of about 1.15 mm). Preferably, the cut rag tobacco has a cut width at or below 40 cuts per inch (about 15.7 cuts per cm, equivalent to a cut width of about 0.64 mm). Cut widths between 0.5 mm and 2.0 mm, for instance between 0.6 mm and 1.5 mm, or between 0.6 mm and 1.7 mm, have been found to result in tobacco material which is preferable in terms of surface area to volume ratio, particularly when heated, and the overall density and pressure drop of the substrate 3. The cut rag tobacco can be formed from a mixture of forms of tobacco material, for instance a mixture of leaf tobacco and one or more of paper reconstituted tobacco, extruded tobacco and bandcast tobacco. Preferably the tobacco material comprises paper reconstituted tobacco.

The leaf tobacco and/or the paper reconstituted tobacco material may comprise a width of between about 0.5 mm and about 2 mm, between about 0.6 mm and about 1.75 mm, between about 0.6 mm and about 1.7 mm or between about 0.7 and about 1.5 mm.

In the tobacco compositions described herein, the tobacco composition may comprise a filler component. The filler component is generally a non-tobacco component, that is, a component that does not include ingredients originating from tobacco. The filler component may be a non-tobacco fiber such as wood fiber or pulp or wheat fiber. The filler component may also be an inorganic material such as chalk, perlite, vermiculite, diatomaceous earth, colloidal silica, magnesium oxide, magnesium sulphate, magnesium carbonate. The filler component may also be a non-tobacco cast material or a non-tobacco extruded material.

The filler component may be present in an amount of 0 to 20% by weight of the tobacco material, or in an amount of from 1 to 10% by weight of the composition. In a preferred embodiment, the tobacco composition comprises between about 5% and about 10% by weight of the tobacco composition. In some embodiments, the filler component is absent.

Extruded tobacco may optionally be included in the tobacco compositions described herein. If extruded tobacco is included, it may be present, for example, in an amount of from 10 to 30% by weight, or 10 to 20% by weight, of the tobacco component. The extruded tobacco which may be used in the tobacco compositions described herein may be prepared by methods which are known to those skilled in the art for preparing extruded tobacco. In some embodiments, extruded tobacco can be prepared as follows. The tobacco furnish may include Virginia (flue cured) tobacco. Burley tobacco, and/or Oriental tobacco. The tobacco furnish may be stems, scraps, strips, fines, or winnowings. Additional components may include non-tobacco fiber, such as straw fiber or wheat fibers: binders, for example celluloses or modified celluloses such as hydroxypropyl cellulose and carboxymethylcellulose; and casings, for example acids such as malic acid.

As shown in FIG. 2, the tobacco furnish and any additional components are mixed in a mixing silo, and conveyed by a dosing screw and conveyor screw to an extruder, where they are mixed with water, and at this stage an aerosol forming material may also be added. After extrusion, the extruded tobacco is cooled on a cooling belt.

An analogous material to those described above in the section, but made using only non-tobacco fibers, such as wheat fiber or wood fiber, may be used in the filler component of the tobacco composition.

According to some embodiments of an aspect of the disclosure, there is provided a method of manufacturing the tobacco composition as described herein, wherein the method comprises applying an aerosol forming material as described herein to the leaf tobacco material.

The method may comprise combining the leaf tobacco material with paper reconstitute tobacco material comprising aerosol forming material in an amount of between 10% and 20% by weight of the paper reconstitute tobacco material.

As shown in FIG. 3, the tobacco composition may be manufactured by a method comprising applying the aerosol forming material to the leaf tobacco and then combining the leaf tobacco comprising the aerosol forming material with the reconstituted tobacco material.

For example, the aerosol forming material may be applied to the leaf tobacco by spraying it onto the leaf tobacco or by soaking the leaf tobacco in the aerosol forming material. Alternatively or in addition, the tobacco composition may be manufactured by applying the aerosol forming material to the reconstituted tobacco material.

According to embodiments of an aspect of the disclosure there is provided a tobacco composition manufactured by the methods described herein.

According to embodiments of an aspect of the disclosure, the tobacco compositions described herein are used in an article for use with an aerosol generation device. The tobacco compositions may be used in a process for manufacturing an article for use with an aerosol generation device.

According to embodiments of an aspect of the disclosure, there is provided an article for use with an aerosol generation device comprising a tobacco composition as described herein. The article for use with an aerosol generation device comprises a rod of the tobacco composition. The rod may have a total weight of between about 250 mg and about 350 mg.

In an embodiment, the tobacco composition may be wrapped in a wrapper having a permeability of less than 100 Coresta Units.

The article for use with an aerosol generation device may comprise reconstituted tobacco material having a density of less than about 700 milligrams per cubic centimeter.

The article for use with an aerosol generation device may have an outer circumference of at least about 19 mm, preferably between about 19 mm and about 23 mm or about 21 mm. This may facilitate insertion of the article for use with an aerosol generation device into the aerosol generation device.

According to embodiments of an aspect of the disclosure, there is provided a system comprising a tobacco composition as described herein and a device arranged to heat the tobacco composition and generate an aerosol from the tobacco composition.

In some embodiments, the system comprises an article for use with an aerosol generation device as described herein and the aerosol generation device is arranged to receive at least a portion of the article for use with an aerosol generation device comprising the tobacco composition and to heat the portion of the article for use with an aerosol generation device comprising the tobacco composition and generate an aerosol from the tobacco composition.

FIG. 4 is a side-on cross sectional view of an article 1 for use with a non-combustible aerosol provision device.

The article 1 comprises a mouthpiece 2, and a cylindrical rod of aerosol generating material 3, in the present case tobacco material, connected to the mouthpiece 2. The aerosol generating material 3, also referred to herein as an aerosol generating substrate 3, comprises at least one aerosol forming material. In the present example, the aerosol forming material is glycerol. In alternative examples, the aerosol forming material can be another material as described herein or a combination thereof. The aerosol forming material has been found to improve the sensory performance of the article, by helping to transfer compounds such as flavor compounds from the aerosol generating material to the consumer. However, an issue with adding such aerosol forming materials to the aerosol generating material within an article for use in a non-combustible aerosol provision system can be that, when the aerosol forming material is aerosolized upon heating, it can increase the mass of aerosol which is delivered by the article, and this increased mass can maintain a higher temperature as it passes through the mouthpiece. As it passes through the mouthpiece, the aerosol transfers heat into the mouthpiece and this warms the outer surface of the mouthpiece, including the area which comes into contact with the consumers lips during use. The mouthpiece temperature can be significantly higher than consumers may be accustomed to when smoking, for instance, conventional cigarettes, and this can be an undesirable effect caused by the use of such aerosol forming materials.

The part of the mouthpiece which comes into contact with a consumer's lips has usually been a paper tube, which is either hollow or surrounds a cylindrical body of filter material.

As shown in FIG. 4, the mouthpiece 2 of the article 1 comprises an upstream end 2 a adjacent to the aerosol generating substrate 3 and a downstream end 2 b distal from the aerosol generating substrate 3. At the downstream end 2 b, the mouthpiece 2 has a hollow tubular element 4 formed from filamentary tow. This has advantageously been found to significantly reduce the temperature of the outer surface of the mouthpiece 2 at the downstream end 2 b of the mouthpiece which comes into contact with a consumer's mouth when the article 1 is in use. In addition, the use of the tubular element 4 has also been found to significantly reduce the temperature of the outer surface of the mouthpiece 2 even upstream of the tubular element 4. Without wishing to be bound by theory, it is hypothesized that this is due to the tubular element 4 channeling aerosol closer to the center of the mouthpiece 2, and therefore reducing the transfer of heat from the aerosol to the outer surface of the mouthpiece 2.

In the present example, the article 1 has an outer circumference of about 21 mm (i.e. the article is in the demi-slim format). In other examples, the article can be provided in any of the formats described herein, for instance having an outer circumference of between 15 mm and 25 mm. Since the article is to be heated to release an aerosol, improved heating efficiency can be achieved using articles having lower outer circumferences within this range, for instance circumferences of less than 23 mm. To achieve improved aerosol via heating, while maintaining a suitable product length, article circumferences of greater than 19 mm have also been found to be particularly effective. Articles having circumferences of between 19 mm and 23 mm, and more preferably between 20 mm and 22 mm, have been found to provide a good balance between providing effective aerosol delivery while allowing for efficient heating.

The outer circumference of the mouthpiece 2 is substantially the same as the outer circumference of the rod of aerosol generating material 3, such that there is a smooth transition between these components. In the present example, the outer circumference of the mouthpiece 2 is about 20.8 mm. A tipping paper 5 is wrapped around the full length of the mouthpiece 2 and over part of the rod of aerosol generating material 3 and has an adhesive on its inner surface to connect the mouthpiece 2 and rod 3. In the present example, the tipping paper 5 extends 5 mm over the rod of aerosol generating material 3 but it can alternatively extend between 3 mm and 10 mm over the rod 3, or more preferably between 4 mm and 6 mm, to provide a secure attachment between the mouthpiece 2 and rod 3. The tipping paper 5 can have a basis weight which is higher than the basis weight of plug wraps used in the article 1, for instance a basis weight of 40 gsm to 80 gsm, more preferably between 50 gsm and 70 gsm, and in the present example 58 gsm. These ranges of basis weights have been found to result in tipping papers having acceptable tensile strength while being flexible enough to wrap around the article 1 and adhere to itself along a longitudinal lap seam on the paper. The outer circumference of the tipping paper 5, once wrapped around the mouthpiece 2, is about 21 mm.

The “wall thickness” of the hollow tubular element 4 corresponds to the thickness of the wall of the tube 4 in a radial direction. This may be measured, for example, using a caliper. The wall thickness is advantageously greater than 0.9 mm, and more preferably 1.0 mm or greater. Preferably, the wall thickness is substantially constant around the entire wall of the hollow tubular element 4. However, where the wall thickness is not substantially constant, the wall thickness is preferably greater than 0.9 mm at any point around the hollow tubular element 4, more preferably 1.0 mm or greater.

Preferably, the length of the hollow tubular element 4 is less than about 20 mm. More preferably, the length of the hollow tubular element 4 is less than about 15 mm. Still more preferably, the length of the hollow tubular element 4 is less than about 10 mm. In addition, or as an alternative, the length of the hollow tubular element 4 is at least about 5 mm. Preferably, the length of the hollow tubular element 4 is at least about 6 mm. In some preferred embodiments, the length of the hollow tubular element 4 is from about 5 mm to about 20 mm, more preferably from about 6 mm to about 10 mm, even more preferably from about 6 mm to about 8 mm, most preferably about 6 mm, 7 mm or about 8 mm. In the present example, the length of the hollow tubular element 4 is 6 mm.

Preferably, the density of the hollow tubular element 4 is at least about 0.25 grams per cubic centimeter (g/cc), more preferably at least about 0.3 g/cc. Preferably, the density of the hollow tubular element 4 is less than about 0.75 grams per cubic centimeter (g/cc), more preferably less than 0.6 g/cc. In some embodiments, the density of the hollow tubular element 4 is between 0.25 and 0.75 g/cc, more preferably between 0.3 and 0.6 g/cc, and more preferably between 0.4 g/cc and 0.6 g/cc or about 0.5 g/cc. These densities have been found to provide a good balance between improved firmness afforded by denser material and the lower heat transfer properties of lower density material. For the purposes of the present disclosure, the “density” of the hollow tubular element 4 refers to the density of the filamentary tow forming the element with any plasticizer incorporated. The density may be determined by dividing the total weight of the hollow tubular element 4 by the total volume of the hollow tubular element 4, wherein the total volume can be calculated using appropriate measurements of the hollow tubular element 4 taken, for example, using calipers. Where necessary, the appropriate dimensions may be measured using a microscope.

The filamentary tow forming the hollow tubular element 4 preferably has a total denier of less than 45,000, more preferably less than 42,000. This total denier has been found to allow the formation of a tubular element 4 which is not too dense. Preferably, the total denier is at least 20,000, more preferably at least 25,000. In preferred embodiments, the filamentary tow forming the hollow tubular element 4 has a total denier between 25,000 and 45,000, more preferably between 35.000 and 45,000. Preferably the cross-sectional shape of the filaments of tow are ‘Y’ shaped, although in other embodiments other shapes such as ‘X’ shaped filaments can be used.

The filamentary tow forming the hollow tubular element 4 preferably has a denier per filament of greater than 3. This denier per filament has been found to allow the formation of a tubular element 4 which is not too dense. Preferably, the denier per filament is at least 4, more preferably at least 5. In preferred embodiments, the filamentary tow forming the hollow tubular element 4 has a denier per filament between 4 and 10, more preferably between 4 and 9. In one example, the filamentary tow forming the hollow tubular element 4 has an 8Y 40,000 tow formed from cellulose acetate and comprising 18% plasticizer, for instance triacetin.

The hollow tubular element 4 preferably has an internal diameter of greater than 3.0 mm. Smaller diameters than this can result in increasing the velocity of aerosol passing though the mouthpiece 2 to the consumer's mouth more than is desirable, such that the aerosol becomes too warm, for instance reaching temperatures greater than 40° C. or greater than 45° C. More preferably, the hollow tubular element 4 has an internal diameter of greater than 3.1 mm, and still more preferably greater than 3.5 mm or 3.6 mm. In one embodiment, the internal diameter of the hollow tubular element 4 is about 3.9 mm.

The hollow tubular element 4 preferably comprises from 15% to 22% by weight of plasticizer. For cellulose acetate tow, the plasticizer is preferably triacetin, although other plasticizers such as polyethylene glycol (PEG) can be used. More preferably, the tubular element 4 comprises from 16% to 20% by weight of plasticizer, for instance about 17%, about 18% or about 19% plasticizer.

The pressure drop or difference (also referred to a resistance to draw) across the mouthpiece, for instance the part of the article 1 downstream of the aerosol generating material 3, is preferably less than about 40 mmH₂O. Such pressure drops have been found to allow sufficient aerosol, including desirable compounds such as flavor compounds, to pass through the mouthpiece 2 to the consumer. More preferably, the pressure drop across the mouthpiece 2 is less than about 32mmH₂O. In some embodiments, particularly improved aerosol has been achieved using a mouthpiece 2 having a pressure drop of less than 31 mmH₂O, for instance about 29 mmH₂O, about 28 mmH₂O or about 27.5 mmH₂O. Alternatively or additionally, the mouthpiece pressure drop can be at least 10 mmH₂O, preferably at least 15 mmH₂O and more preferably at least 20 mmH₂O. In some embodiments, the mouthpiece pressure drop can be between about 15 mmH₂O and 40 mmH₂O. These values enable the mouthpiece 2 to slow down the aerosol as it passes through the mouthpiece 2 such that the temperature of the aerosol has time to reduce before reaching the downstream end 2 b of the mouthpiece 2.

The mouthpiece 2, in the present example, includes a body of material 6 upstream of the hollow tubular element 4, in this example adjacent to and in an abutting relationship with the hollow tubular element 4. The body of material 6 and hollow tubular element 4 each define a substantially cylindrical overall outer shape and share a common longitudinal axis. The body of material 6 is wrapped in a first plug wrap 7. Preferably, the first plug wrap 7 has a basis weight of less than 50 gsm, more preferably between about 20 gsm and 40 gsm. Preferably, the first plug wrap 7 has a thickness of between 30 μm and 60 μm, more preferably between 35 μm and 45 μm. Preferably, the first plug wrap 7 is a non-porous plug wrap, for instance having a permeability of less than 100 Coresta units, for instance less than 50 Coresta units. However, in other embodiments, the first plug wrap 7 can be a porous plug wrap, for instance having a permeability of greater than 200 Coresta Units.

Preferably, the length of the body of material 6 is less than about 15 mm. More preferably, the length of the body of material 6 is less than about 10 mm. In addition, or as an alternative, the length of the body of material 6 is at least about 5 mm.

Preferably, the length of the body of material 6 is at least about 6 mm. In some preferred embodiments, the length of the body of material 6 is from about 5 mm to about 15 mm, more preferably from about 6 mm to about 12 mm, even more preferably from about 6 mm to about 12 mm, most preferably about 6 mm, 7 mm, 8 mm, 9 mm or 10 mm. In the present example, the length of the body of material 6 is 10 mm. In the present example, the body of material 6 is formed from filamentary tow. In the present example, the tow used in the body of material 6 has a denier per filament (d.p.f.) of 8.4 and a total denier of 21,000. Alternatively, the tow can, for instance, have a denier per filament (d.p.f.) of 9.5 and a total denier of 12,000. In the present example, the tow comprises plasticized cellulose acetate tow. The plasticizer used in the tow comprises about 7% by weight of the tow. In the present example, the plasticizer is triacetin. In other examples, different materials can be used to form the body of material 6. For instance, rather than tow, the body 6 can be formed from paper, for instance in a similar way to paper filters known for use in cigarettes.

Alternatively, the body 6 can be formed from tows other than cellulose acetate, for instance polylactic acid (PLA), other materials described herein for filamentary tow or similar materials. The tow is preferably formed from cellulose acetate. The tow, whether formed from cellulose acetate or other materials, preferably has a d.p.f. of at least 5, more preferably at least 6 and still more preferably at least 7. These values of denier per filament provide a tow which has relatively coarse, thick fibers with a lower surface area which result in a lower pressure drop across the mouthpiece 2 than tows having lower d.p.f. values. Preferably, to achieve a sufficiently uniform body of material 6, the tow has a denier per filament of no more than 12 d.p.f., preferably no more than 11 d.p.f. and still more preferably no more than 10 d.p.f.

The total denier of the tow forming the body of material 6 is preferably at most 30,000, more preferably at most 28,000 and still more preferably at most 25,000. These values of total denier provide a tow which takes up a reduced proportion of the cross sectional area of the mouthpiece 2 which results in a lower pressure drop across the mouthpiece 2 than tows having higher total denier values. For appropriate firmness of the body of material 6, the tow preferably has a total denier of at least 8,000 and more preferably at least 10,000. Preferably, the denier per filament is between 5 and 12 while the total denier is between 10,000 and 25,000. More preferably, the denier per filament is between 6 and 10 while the total denier is between 11,000 and 22,000. Preferably the cross-sectional shape of the filaments of tow are ‘Y’ shaped, although in other embodiments other shapes such as ‘X’ shaped filaments can be used, with the same d.p.f. and total denier values as provided herein.

In the present example the hollow tubular element 4 is a first hollow tubular element 4 and the mouthpiece includes a second hollow tubular element 8, also referred to as a cooling element, upstream of the first hollow tubular element 4. In the present example, the second hollow tubular element 8 is upstream of, adjacent to and in an abutting relationship with the body of material 6. The body of material 6 and second hollow tubular element 8 each define a substantially cylindrical overall outer shape and share a common longitudinal axis. The second hollow tubular element 8 is formed from a plurality of layers of paper which are parallel wound, with butted seams, to form the tubular element 8. In the present example, first and second paper layers are provided in a two-ply tube, although in other examples 3, 4 or more paper layers can be used forming 3, 4 or more ply tubes. Other constructions can be used, such as spirally wound layers of paper, cardboard tubes, tubes formed using a papier-mâché type process, molded or extruded plastic tubes or similar. The second hollow tubular element 8 can also be formed using a stiff plug wrap and/or tipping paper as the second plug wrTap 9 and/or tipping paper 5 described herein, meaning that a separate tubular element is not required. The stiff plug wrap and/or tipping paper is manufactured to have a rigidity that is sufficient to withstand the axial compressive forces and bending moments that might arise during manufacture and whilst the article 1 is in use. For instance, the stiff plug wrap and/or tipping paper can have a basis weight between 70 gsm and 120 gsm, more preferably between 80 gsm and 110 gsm. Additionally or alternatively, the stiff plug wrap and/or tipping paper can have a thickness between 80 μm and 200 μm, more preferably between 100 μm and 160 μm, or from 120 μm to 150 μm. It can be desirable for both the second plug wrap 9 and tipping paper 5 to have values in these ranges, to achieve an acceptable overall level of rigidity for the second hollow tubular element 8.

The second hollow tubular element 8 preferably has a wall thickness, which can be measured in the same way as that of the first hollow tubular element 4, of at least about 100 μm and up to about 1.5 mm, preferably between 100 μm and 1 mm and more preferably between 150 μm and 500 μm, or about 300 μm. In the present example, the second hollow tubular element 8 has a wall thickness of about 290 μm.

Preferably, the length of the second hollow tubular element 8 is less than about 50 mm. More preferably, the length of the second hollow tubular element 8 is less than about 40 mm. Still more preferably, the length of the second hollow tubular element 8 is less than about 30 mm. In addition, or as an alternative, the length of the second hollow tubular element 8 is preferably at least about 10 mm. Preferably, the length of the second hollow tubular element 8 is at least about 15 mm. In some preferred embodiments, the length of the second hollow tubular element 8 is from about 20 mm to about 30 mm, more preferably from about 22 mm to about 28 mm, even more preferably from about 24 to about 26 mm, most preferably about 25 mm. In the present example, the length of the second hollow tubular element 8 is 25 mm.

The second hollow tubular element 8 is located around and defines an air gap within the mouthpiece 2 which acts as a cooling segment. The air gap provides a chamber through which heated volatilized components generated by the aerosol generating material 3 flow. The second hollow tubular element 8 is hollow to provide a chamber for aerosol accumulation yet rigid enough to withstand axial compressive forces and bending moments that might arise during manufacture and whilst the article 1 is in use. The second hollow tubular element 8 provides a physical displacement between the aerosol generating material 3 and the body of material 6. The physical displacement provided by the second hollow tubular element 8 will provide a thermal gradient across the length of the second hollow tubular element 8.

Preferably, the mouthpiece 2 comprises a cavity having an internal volume greater than 450 mm³. Providing a cavity of at least this volume has been found to enable the formation of an improved aerosol. Such a cavity size provides sufficient space within the mouthpiece 2 to allow heated volatilized components to cool, therefore allowing the exposure of the aerosol generating material 3 to higher temperatures than would otherwise be possible, since they may result in an aerosol which is too warm. In the present example, the cavity is formed by the second hollow tubular element 8, but in alternative arrangements it could be formed within a different part of the mouthpiece 2. More preferably, the mouthpiece 2 comprises a cavity, for instance formed within the second hollow tubular element 8, having an internal volume greater than 500 mm³, and still more preferably greater than 550 mm³, allowing further improvement of the aerosol. In some examples, the internal cavity comprises a volume of between about 550 mm³ and about 750 mm³, for instance about 600 mm³ or 700 mm³.

The second hollow tubular element 8 can be configured to provide a temperature differential of at least 40 degrees Celsius between a heated volatilized component entering a first, upstream end of the second hollow tubular element 8 and a heated volatilized component exiting a second, downstream end of the second hollow tubular element 8. The second hollow tubular element 8 is preferably configured to provide a temperature differential of at least 60 degrees Celsius, preferably at least 80 degrees Celsius and more preferably at least 100 degrees Celsius between a heated volatilized component entering a first, upstream end of the second hollow tubular element 8 and a heated volatilized component exiting a second, downstream end of the second hollow tubular element 8. This temperature differential across the length of the second hollow tubular element 8 protects the temperature sensitive body of material 6 from the high temperatures of the aerosol generating material 3 when it is heated.

In alternative articles, the second hollow tubular element 8 can be replaced with an alternative cooling element, for instance an element formed from a body of material which allows aerosol to pass through it longitudinally, and which also performs the function of cooling the aerosol.

In the present example, the first hollow tubular element 4, body of material 6 and second hollow tubular element 8 are combined using a second plug wrap 9 which is wrapped around all three sections. Preferably, the second plug wrap 9 has a basis weight of less than 50 gsm, more preferably between about 20 gsm and 45 gsm. Preferably, the second plug wrap 9 has a thickness of between 30 μm and 60 μm, more preferably between 35 μm and 45 μm. The second plug wrap 9 is preferably a non-porous plug wrap having a permeability of less than 100 Coresta Units, for instance less than 50 Coresta Units. However, in alternative embodiments, the second plug wrap 9 can be a porous plug wrap, for instance having a permeability of greater than 200 Coresta Units.

In the present example, the aerosol generating material 3 is wrapped in a wrapper 10. The wrapper 10 can, for instance, be a paper or paper-backed foil wrapper. In the present example, the wrapper 10 is substantially impermeable to air. In alternative embodiments, the wrapper 10 preferably has a permeability of less than 100 Coresta Units, more preferably less than 60 Coresta Units. It has been found that low permeability wrappers, for instance having a permeability of less than 100 Coresta Units, more preferably less than 60 Coresta Units, result in an improvement in the aerosol formation in the aerosol generating material 3. Without wishing to be bound by theory, it is hypothesized that this is due to reduced loss of aerosol compounds through the wrapper 10. The permeability of the wrapper 10 can be measured in accordance with ISO 2965:2009 concerning the determination of air permeability for materials used as cigarette papers, filter plug wrap and filter joining paper.

In the present embodiment, the wrapper 10 comprises aluminum foil. Aluminum foil has been found to be particularly effective at enhancing the formation of aerosol within the aerosol generating material 3. In the present example, the aluminum foil has a metal layer having a thickness of about 6 μm. In the present example, the aluminum foil has a paper backing. However, in alternative arrangements, the aluminum foil can be other thicknesses, for instance between 4 μm and 16 μm in thickness. The aluminum foil also need not have a paper backing, but could have a backing formed from other materials, for instance to help provide an appropriate tensile strength to the foil, or it could have no backing material.

Metallic layers or foils other than aluminum can also be used. The total thickness of the wrapper is preferably between 20 μm and 60 μm, more preferably between 30 μm and 50 μm, which can provide a wrapper having appropriate structural integrity and heat transfer characteristics. The tensile force which can be applied to the wrapper before it breaks can be greater than 3,000 grams force, for instance between 3,000 and 10,000 grams force or between 3,000 and 4,500 grams force.

The article has a ventilation level of about 75% of the aerosol drawn through the article. In alternative embodiments, the article can have a ventilation level of between 50% and 80% of aerosol drawn through the article, for instance between 65% and 75%. Ventilation at these levels helps to slow down the flow of aerosol drawn through the mouthpiece 2 and thereby enable the aerosol to cool sufficiently before it reaches the downstream end 2 b of the mouthpiece 2. The ventilation is provided directly into the mouthpiece 2 of the article 1. In the present example, the ventilation is provided into the second hollow tubular element 8, which has been found to be particularly beneficial in assisting with the aerosol generation process. The ventilation is provided via first and second parallel rows of perforations 12, in the present case formed as laser perforations, at positions 17.925 mm and 18.625 mm respectively from the downstream, mouth-end 2 b of the mouthpiece 2. These perforations pass though the tipping paper 5, second plug wrap 9 and second hollow tubular element 8. In alternative embodiments, the ventilation can be provided into the mouthpiece at other locations, for instance into the body of material 6 or first tubular element 4.

In the present example, the aerosol forming material added to the aerosol generating substrate 3 comprises 14% by weight of the aerosol generating substrate 3. Preferably, the aerosol forming material comprises at least 5% by weight of the aerosol generating substrate, more preferably at least 10%. Preferably, the aerosol forming material comprises less than 25% by weight of the aerosol generating substrate, more preferably less than 20%, for instance between 10% and 20%, between 12% and 18% or between 13% and 16%.

Preferably the aerosol generating material 3 is provided as a cylindrical rod of aerosol generating material. Irrespective of the form of the aerosol generating material, it preferably has a length of about 10 mm to 100 mm. In some embodiments, the length of the aerosol generating material is preferably in the range about 25 mm to 50 mm, more preferably in the range about 30 mm to 45 mm, and still more preferably about 30 mm to 40 mm.

The volume of aerosol generating material 3 provided can vary from about 200 mm³ to about 4300 mm³, preferably from about 500 mm³ to 1500 mm³, more preferably from about 1000 mm³ to about 1300 mm³. The provision of these volumes of aerosol generating material, for instance from about 1000 mm³ to about 1300 mm³, has been advantageously shown to achieve a superior aerosol, having a greater visibility and sensory performance compared to that achieved with volumes selected from the lower end of the range.

The mass of aerosol generating material 3 provided can be greater than 200 mg, for instance from about 200 mg to 400 mg, preferably from about 230 mg to 360 mg, more preferably from about 250 mg to 360 mg. It has been advantageously found that providing a higher mass of aerosol generating material results in improved sensory performance compared to aerosol generated from a lower mass of tobacco material.

Preferably the aerosol generating material or substrate is formed from tobacco material as described herein, which includes a tobacco component.

FIG. 5a is a side-on cross sectional view of a further article 1′ including a capsule-containing mouthpiece 2′. FIG. 5b is a cross sectional view of the capsule-containing mouthpiece shown in FIG. 5a through the line A-A′ thereof. Article 1′ and capsule-containing mouthpiece 2′ are the same as the article 1 and mouthpiece 2 illustrated in FIG. 4, except that an aerosol modifying agent is provided within the body of material 6, in the present example in the form of a capsule 11, and that an oil-resistant first plug wrap 7′ surrounds the body of material 6. In other examples, the aerosol modifying agent can be provided in other forms, such as material injected into the body of material 6 or provided on a thread, for instance the thread carrying a flavorant or other aerosol modifying agent, which may also be disposed within the body of material 6.

The capsule 11 can comprise a breakable capsule, for instance a capsule which has a solid, frangible shell surrounding a liquid payload. In the present example, a single capsule 11 is used. The capsule 11 is entirely embedded within the body of material 6. In other words, the capsule 11 is completely surrounded by the material forming the body 6. In other examples, a plurality of breakable capsules may be disposed within the body of material 6, for instance 2, 3 or more breakable capsules. The length of the body of material 6 can be increased to accommodate the number of capsules required. In examples where a plurality of capsules is used, the individual capsules may be the same as each other, or may differ from one another in terms of size and/or capsule payload. In other examples, multiple bodies of material 6 may be provided, with each body containing one or more capsules.

The capsule 11 has a core-shell structure. In other words, the capsule 11 comprises a shell encapsulating a liquid agent, for instance a flavorant or other agent, which can be any one of the flavorants or aerosol modifying agents described herein. The shell of the capsule can be ruptured by a user to release the flavorant or other agent into the body of material 6. The first plug wrap T can comprise a barrier coating to make the material of the plug wrap substantially impermeable to the liquid payload of the capsule 11. Alternatively or in addition, the second plug wrap 9 and/or tipping paper 5 can comprise a barrier coating to make the material of that plug wrap and/or tipping paper substantially impermeable to the liquid payload of the capsule 11.

In the present example, the capsule 11 is spherical and has a diameter of about 3 mm. In other examples, other shapes and sizes of capsule can be used. The total weight of the capsule 11 may be in the range about 10 mg to about 50 mg.

In the present example, the capsule 11 is located at a longitudinally central position within the body of material 6. That is, the capsule 11 is positioned so that its center is 4 mm from each end of the body of material 6. In other examples, the capsule 11 can be located at a position other than a longitudinally central position in the body of material 6, i.e. closer to the downstream end of the body of material 6 than the upstream end, or closer to the upstream end of the body of material 6 than the downstream end. Preferably, the mouthpiece 2′ is configured so that the capsule 11 and the ventilation holes 12 are longitudinally offset from each other in the mouthpiece 2′.

A cross section of the mouthpiece 2′ is shown in FIG. 5b , this being taken through line A-A′ of FIG. 5a . FIG. 5b shows the capsule 11, the body of material 6, the first and second plug wraps 7′, 9 and the tipping paper 5. In the present example, the capsule 11 is centered on the longitudinal axis (not shown) of the mouthpiece 2′. The first and second plug wraps 7′, 9 and tipping 5 are arranged concentrically around the body of material 6.

The breakable capsule 11 has a core-shell structure. That is, the encapsulating material or barrier material creates a shell around a core that comprises the aerosol modifying agent. The shell structure hinders migration of the aerosol modifying agent during storage of the article 1′ but allows controlled release of the aerosol modifying agent, also referred to as an aerosol modifier, during use.

In some cases, the barrier material (also referred to herein as the encapsulating material) is frangible. The capsule is crushed or otherwise fractured or broken by the user to release the encapsulated aerosol modifier. Typically, the capsule is broken immediately prior to heating being initiated but the user can select when to release the aerosol modifier. The term “breakable capsule” refers to a capsule, wherein the shell can be broken by means of a pressure to release the core; more specifically the shell can be ruptured under the pressure imposed by the user's fingers when the user wants to release the core of the capsule.

In some cases, the barrier material is heat resistant. That is to say, in some cases, the barrier will not rupture, melt or otherwise fail at the temperature reached at the capsule site during operation of the aerosol provision device. Illustratively, a capsule located in a mouthpiece may be exposed to temperatures in the range of 30° C. to 100° C. for example, and the barrier material may continue to retain the liquid core up to at least about 50° C. to 120° C.

In other cases, the capsule releases the core composition on heating, for example by melting of the barrier material or by capsule swelling leading to rupture of the barrier material.

The total weight of a capsule may be in the range of about 1 mg to about 100 mg, suitably about 5 mg to about 60 mg, about 8 mg to about 50 mg, about 10 mg to about 20 mg, or about 12 mg to about 18 mg.

The total weight of the core formulation may be in the range of about 2 mg to about 90 mg, suitably about 3 mg to about 70 mg, about 5 mg to about 25 mg, about 8 mg to about 20 mg, or about 10 mg to about 15 mg.

The capsule according to the disclosure comprises a core as described above, and a shell. The capsules may present a crush strength from about 4.5 N to about 40 N, more preferably from about 5 N to about 30 N or to about 28 N (for instance about 9.8 N to about 24.5 N). The capsule burst strength can be measured when the capsule is removed from the body of material 6 and using a force gauge to measure the force at which the capsule bursts when pressed between two flat metal plates. A suitable measurement device is the Sauter FK 50 force gauge with a flat headed attachment, which can be used to crush the capsule against a flat, hard surface having a surface similar to the attachment.

The capsules may be substantially spherical and have a diameter of at least about 0.4 mm, 0.6 mm, 0.8 mm, 1.0 mm, 2.0 mm, 2.5 mm, 2.8 mm or 3.0 mm. The diameter of the capsules may be less than about 10.0 mm, 8.0 mm, 7.0 mm, 6.0 mm, 5.5 mm, 5.0 mm, 4.5 mm, 4.0 mm, 3.5 mm or 3.2 mm. Illustratively, the capsule diameter may be in the range of about 0.4 mm to about 10.0 mm, about 0.8 mm to about 6.0 mm, about 2.5 mm to about 5.5 mm or about 2.8 mm to about 3.2 mm. In some cases, the capsule may have a diameter of about 3.0 mm. These sizes are particularly suitable for incorporation of the capsule into an article as described herein.

The cross-sectional area of the capsule 11 at its largest cross sectional area is in some embodiments less than 28% of the cross sectional area of the portion of the mouthpiece 2′ in which the capsule 11 is provided, more preferably less than 27% and still more preferably less than 25%. For instance, for the spherical capsule having a diameter of 3.0 mm, the largest cross sectional area of the capsule is 7.07 mm². For the mouthpiece 2′ having a circumference of 21 mm as described herein, the body of material 6 has an outer circumference of 20.8 mm, and the radius of this component will be 3.31 mm, corresponding to a cross sectional area of 34.43 mm². The capsule cross sectional area is, in this example, 20.5% of the cross-sectional area of the mouthpiece 2′. As another example, if the capsule had a diameter of 3.2 mm, its largest cross sectional area would be 8.04 mm². In this case, the cross sectional area of the capsule would be 23.4% of the cross sectional area of the body of material 6. A capsule with a largest cross sectional area less than 28% of the cross sectional area of the portion of the mouthpiece 2′ in which the capsule 11 is provided has the advantage that the pressure drop across the mouthpiece 2′ is reduced as compared to capsules with larger cross sectional areas and adequate space remains around the capsule for aerosol to pass without the body of material 6 removing significant amounts of the aerosol mass as it passes through the mouthpiece 2′.

Preferably the pressure drop or difference (also referred to a resistance to draw) across the article, measured as the open pressure drop (i.e. with the ventilation openings open), reduces by less than 8 mmH₂O when the capsule is broken. More preferably, the open pressure drop reduces by less than 6 mmH₂O and more preferably less than 5 mmH₂O. These values are measured as the average achieved by at least 80 articles made to the same design. Such small changes in pressure drop mean that other aspects of the product design, such as setting the correct ventilation level for a given product pressure drop, can be achieved irrespective of whether or not the consumer chooses to break the capsule.

The barrier material may comprise one or more of a gelling agent, a bulking agent, a buffer, a coloring agent and a plasticizer.

Suitably, the gelling agent may be, for example, a polysaccharide or cellulosic gelling agent, a gelatin, a gum, a gel, a wax or a mixture thereof. Suitable polysaccharides include alginates, dextrans, maltodextrins, cyclodextrins and pectins. Suitable alginates include, for instance, a salt of alginic acid, an esterified alginate or glyceryl alginate. Salts of alginic acid include ammonium alginate, triethanolamine alginate, and group I or II metal ion alginates like sodium, potassium, calcium and magnesium alginate. Esterified alginates include propylene glycol alginate and glyceryl alginate. In an embodiment, the barrier material is sodium alginate and/or calcium alginate. Suitable cellulosic materials include methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose, cellulose acetate and cellulose ethers. The gelling agent may comprise one or more modified starches. The gelling agent may comprise carrageenans. Suitable gums include agar, gellan gum, gum Arabic, pullulan gum, mannan gum, gum ghatti, gum tragacanth, Karaya, locust bean, acacia gum, guar, quince seed and xanthan gums. Suitable gels include agar, agarose, carrageenans, furoidan and furcellaran. Suitable waxes include camauba wax. In some cases, the gelling agent may comprise carrageenans and/or gellan gum; these gelling agents are particularly suitable for inclusion as the gelling agent as the pressure required to break the resulting capsules is particularly suitable.

The barrier material may comprise one or more bulking agents, such as starches, modified starches (such as oxidized starches) and sugar alcohols such as maltitol.

The barrier material may comprise a coloring agent which renders easier the location of the capsule within the aerosol generating device during the manufacturing process of the aerosol generating device. The coloring agent is preferably chosen among colorants and pigments.

The barrier material may further comprise at least one buffer, such as a citrate or phosphate compound.

The barrier material may further comprise at least one plasticizer, which may be glycerol, sorbitol, maltitol, triacetin, polyethylene glycol, propylene glycol or another polyalcohol with plasticizing properties, and optionally one acid of the monoacid, diacid or triacid type, especially citric acid, fumaric acid, malic acid, and the like. The amount of plasticizer ranges from 1% to 30% by weight, preferably from 2% to 15% by weight, and even more preferably from 3 to 10% by weight of the total dry weight of the shell.

The barrier material may also comprise one or more filler materials. Suitable filler materials include comprising starch derivatives such as dextrin, maltodextrin, cyclodextrin (alpha, beta or gamma), or cellulose derivatives such as hydroxypropyl-methylcellulose (HPMC), hydroxypropvlcellulose (HPC), methylcellulose (MC), carboxy-methylcellulose (CMC), polyvinyl alcohol, polvols or mixture thereof. Dextrin is a preferred filler. The amount of filler in the shell is at most 98.5%, preferably from 25 to 95% more preferably from 40 to 80% and even more preferably from 50 to 60% by weight on the total dry weight of the shell.

The capsule shell may additionally comprise a hydrophobic outer layer which reduces the susceptibility of the capsule to moisture-induced degradation. The hydrophobic outer layer is suitably selected from the group comprising waxes, especially carnauba wax, candelilla wax or beeswax, carbowax, shellac (in alcoholic or aqueous solution), ethyl cellulose, hydroxypropyl methyl cellulose, hydroxyl-propylcellulose, latex composition, polyvinyl alcohol, or a combination thereof. More preferably, the at least one moisture barrier agent is ethyl cellulose or a mixture of ethyl cellulose and shellac.

The capsule core comprises the aerosol modifier. This aerosol modifier may be any volatile substance which modifies at least one property of the aerosol. For example, the aerosol substance may modify the pH, the sensorial properties, the water content, the delivery characteristics or the flavor. In some cases, the aerosol modifier may be selected from an acid, a base, water or a flavorant. In some embodiments, the aerosol modifier comprises one or more flavorants.

The flavorant may suitably be licorice, rose oil, vanilla, lemon oil, orange oil, a mint-flavor, suitably menthol and/or a mint oil from any species of the genus Mentha such as peppermint oil and/or spearmint oil, or lavender, fennel or anise.

In some cases, the flavorant comprises menthol.

In some cases, the capsule may comprise at least about 25% w/w flavorant (based on the total weight of the capsule), suitably at least about 30% w/w flavorant, 35% w/w flavorant, 40% w/w flavorant, 45% w/w flavorant or 50% w/w flavorant.

In some cases, the core may comprise at least about 25% w/w flavorant (based on the total weight of the core), suitably at least about 30% w/w flavorant, 35% w/w flavorant, 40% w/w flavorant, 45% w/w flavorant or 50% w/w flavorant. In some cases, the core may comprise less than or equal to about 75% w/w flavorant (based on the total weight of the core), suitably less than or equal to about 65% w/w flavorant, 55% w/w flavorant, or 50% w/w flavorant. Illustratively, the capsule may include an amount of flavorant in the range of 25-75% w/w (based on the total weight of the core), about 35-60% w/w or about 40-55% w/w.

The capsules may include at least about 2 mg, 3 mg or 4 mg of the aerosol modifier, suitably at least about 4.5 mg of the aerosol modifier, 5 mg of the aerosol modifier, 5.5 of mg the aerosol modifier or 6 mg of the aerosol modifier.

In some cases, the consumable comprises at least about 7 mg of the aerosol modifier, suitably at least about 8 mg of the aerosol modifier, 10 mg of the aerosol modifier, 12 mg of the aerosol modifier or 15 mg of the aerosol modifier. The core may also comprise a solvent which dissolves the aerosol modifier.

Any suitable solvent may be used.

Where the aerosol modifier comprises a flavorant, the solvent may suitably comprise short or medium chain fats and oils. For example, the solvent may comprise tri-esters of glycerol such as C2-C12 triglycerides, suitably C6-C10 triglycerides or Cs-C12 triglycerides. For example, the solvent may comprise medium chain triglycerides (MCT—C8-C12), which may be derived from palm oil and/or coconut oil.

The esters may be formed with caprylic acid and/or capric acid. For example, the solvent may comprise medium chain triglycerides which are caprylic triglycerides and/or capric tryglycerides. For example, the solvent may comprise compounds identified in the CAS registry by numbers 73398-61-5, 65381-09-1, 85409-09-2. Such medium chain triglycerides are odorless and tasteless.

The hydrophilic-lipophilic balance (HLB) of the solvent may be in the range of 9 to 13, suitably 10 to 12. Methods of making the capsules include co-extrusion, optionally followed by centrifugation and curing and/or drying. The contents of WO 2007/010407 A2 is incorporated by reference, in its entirety.

In the examples described above, the mouthpieces 2, 2′ each comprise a single body of material 6. In other examples, either the mouthpiece of FIG. 4 or of FIGS. 2a and 2b may include multiple bodies of material. The mouthpieces 2, 2′ may comprise a cavity between the bodies of material.

In some examples, the mouthpiece 2, 2′ downstream of the aerosol generating material 3 can comprise a wrapper, for instance the first or second plug wraps 7, 9, or tipping paper 5, which comprises an aerosol modifying agent as described herein. The aerosol modifying agent may be disposed on an inwardly or outwardly facing surface of the mouthpiece wrapper. For instance, the aerosol modifying agent may be provided on an area of the wrapper, such as an outwardly facing surface of the tipping paper 5, which comes into contact with the consumer's lips during use. By disposing the aerosol modifying agent on the outwardly facing surface of the mouthpiece wrapper, the aerosol modifying agent may be transferred to the consumer's lips during use. Transfer of the aerosol modifying agent to the consumer's lips during use of the article may modify the organoleptic properties (e.g. taste) of the aerosol generated by the aerosol generating substrate 3 or otherwise provide the consumer with an alternative sensory experience. For example, the aerosol modifying agent may impart flavor to the aerosol generated by the aerosol generating substrate 3. The aerosol modifying agent may be at least partially soluble in water such that it is transferred to the user via the consumer's saliva. The aerosol modifying agent may be one that volatilizes by the heat generated by the aerosol provision system. This may facilitate transfer of the aerosol modifying agent to the aerosol generated by the aerosol generating substrate 3.

A non-combustible aerosol provision device is used to heat the aerosol generating material 3 of the articles 1, 1′ described herein. The non-combustible aerosol provision device preferably comprises a coil, since this has been found to enable improved heat transfer to the article 1, 1′ as compared to other arrangements.

In some examples, the coil is configured to, in use, cause heating of at least one electrically-conductive heating element, so that heat energy is conductible from the at least one electrically-conductive heating element to the aerosol generating material to thereby cause heating of the aerosol generating material.

In some examples, the coil is configured to generate, in use, a varying magnetic field for penetrating at least one heating element, to thereby cause induction heating and/or magnetic hysteresis heating of the at least one heating element. In such an arrangement, the or each heating element may be termed a “susceptor” as defined herein. A coil that is configured to generate, in use, a varying magnetic field for penetrating at least one electrically-conductive heating element, to thereby cause induction heating of the at least one electrically-conductive heating element, may be termed an “induction coil” or “inductor coil”.

The device may include the heating element(s), for example electrically-conductive heating element(s), and the heating element(s) may be suitably located or locatable relative to the coil to enable such heating of the heating element(s). The heating element(s) may be in a fixed position relative to the coil. Alternatively, the at least one heating element, for example at least one electrically-conductive heating element, may be included in the article 1, 1′ for insertion into a heating zone of the device, wherein the article 1, 1′ also comprises the aerosol generating material 3 and is removable from the heating zone after use. Alternatively, both the device and such an article 1, 1′ may comprise at least one respective heating element, for example at least one electrically-conductive heating element, and the coil may be to cause heating of the heating element(s) of each of the device and the article when the article is in the heating zone.

In some examples, the coil is helical. In some examples, the coil encircles at least a part of a heating zone of the device that is configured to receive aerosol generating material. In some examples, the coil is a helical coil that encircles at least a part of the heating zone.

In some examples, the device comprises an electrically-conductive heating element that at least partially surrounds the heating zone, and the coil is a helical coil that encircles at least a part of the electrically-conductive heating element. In some examples, the electrically-conductive heating element is tubular. In some examples, the coil is an inductor coil.

In some examples, the use of a coil enables the non-combustible aerosol provision device to reach operational temperature more quickly than a non-coil aerosol provision device. For instance, the non-combustible aerosol provision device including a coil as described above can reach an operational temperature such that a first puff can be provided in less than 30 seconds from initiation of a device heating program, more preferably in less than 25 seconds. In some examples, the device can reach an operational temperature in about 20 seconds from the initiation of a device heating program.

The use of a coil as described herein in the device to cause heating of the aerosol generating material has been found to enhance the aerosol which is produced. For instance, consumers have reported that the aerosol generated by a device including a coil such as that described herein is sensorially closer to that generated in factory made cigarette (FMC) products than the aerosol produced by other non-combustible aerosol provision systems. Without wishing to be bound by theory, it is hypothesized that this is the result of the reduced time to reach the required heating temperature when the coil is used, the higher heating temperatures achievable when the coil is used and/or the fact that the coil enables such systems to simultaneously heat a relatively large volume of aerosol generating material, resulting in aerosol temperatures resembling FMC aerosol temperatures. In FMC products, the burning coal generates a hot aerosol which heats tobacco in the tobacco rod behind the coal, as the aerosol is drawn through the rod. This hot aerosol is understood to release flavor compounds from tobacco in the rod behind the burning coal. A device including a coil as described herein is thought to also be capable of heating aerosol generating material, such as tobacco material described herein, to release flavor compounds, resulting in an aerosol which has been reported to more closely resemble an FMC aerosol.

Using an aerosol provision system including a coil as described herein, for instance an induction coil which heats at least some of the aerosol generating material to at least 200° C., more preferably at least 220° C., can enable the generation of an aerosol from an aerosol generating material that has particular characteristics which are thought to more closely resemble those of an FMC product. For example, when heating an aerosol generating material, including nicotine, using an induction heater, heated to at least 250° C., for a two-second period, under an airflow of at least 1.50 L/m during the period, one or more of the following characteristics has been observed:

-   -   at least 10 μg of nicotine is aerosolized from the aerosol         generating material,     -   the weight ratio in the generated aerosol, of aerosol forming         material to nicotine is at least about 2.5:1, suitably at least         8.5:1;     -   at least 100 μg of the aerosol forming material can be         aerosolized from the aerosol generating material;     -   the mean particle or droplet size in the generated aerosol is         less than about 1000 nm; and     -   the aerosol density is at least 0.1 μg/cc.

In some cases, at least 10 μg of nicotine, suitably at least 30 μg or 40 μg of nicotine, is aerosolized from the aerosol generating material under an airflow of at least 1.50 L/m during the period. In some cases, less than about 200 μg, suitably less than about 150 μg or less than about 125 μg, of nicotine is aerosolized from the aerosol generating material under an airflow of at least 1.50 L/m during the period.

In some cases, the aerosol contains at least 100 μg of the aerosol forming material, suitably at least 200 μg, 500 μg or 1 mg of aerosol forming material is aerosolized from the aerosol generating material under an airflow of at least 1.50 L/m during the period. Suitably, the aerosol forming material may comprise or consist of glycerol.

As defined herein, the term “mean particle or droplet size” refers to the mean size of the solid or liquid components of an aerosol (i.e. the components suspended in a gas). Where the aerosol contains suspended liquid droplets and suspended solid particles, the term refers to the mean size of all components together.

In some cases, the mean particle or droplet size in the generated aerosol may be less than about 900 nm, 800 nm, 700, nm 600 nm, 500 nm, 450 nm or 400 nm. In some cases, the mean particle or droplet size may be more than about 25 nm, 50 nm or 100 nm.

In some cases, the aerosol density generated during the period is at least 0.1 μg/cc. In some cases, the aerosol density is at least 0.2 μg/cc, 0.3 μg/cc or 0.4 μg/cc. In some cases, the aerosol density is less than about 2.5 μg/cc, 2.0 μg/cc, 1.5 μg/cc or 1.0 μg/cc.

The non-combustible aerosol provision device is preferably arranged to heat the aerosol generating material 3 of the article 1, 1′, to a maximum temperature of at least 160° C. Preferably, the non-combustible aerosol provision device is arranged to heat the aerosol forming material 3 of the article 1, 1′, to a maximum temperature of at least about 200° C., or at least about 220° C., or at least about 240° C., more preferably at least about 270° C., at least once during the heating process followed by the non-combustible aerosol provision device.

Using an aerosol provision system including a coil as described herein, for instance an induction coil which heats at least some of the aerosol generating material to at least 200° C., more preferably at least 220° C., can enable the generation of an aerosol from an aerosol generating material in an article 1, 1′ as described herein that has a higher temperature as the aerosol leaves the mouth end of the mouthpiece 2, 2′ than previous devices, contributing to the generation of an aerosol which is considered closer to an FMC product. For instance, the maximum aerosol temperature measured at the mouth-end of the article 1, 1′ can preferably be greater than 50° C., more preferably greater than 55° C. and still more preferably greater than 56° C. or 57° C. Additionally or alternatively, the maximum aerosol temperature measured at the mouth-end of the article 1, 1′ can be less than 62° C., more preferably less than 60° C. and more preferably less than 59° C. In some embodiments, the maximum aerosol temperature measured at the mouth-end of the article 1, 1′ can preferably be between 50° C. and 62° C., more preferably between 56° C. and 60° C.

FIG. 6 shows an example of a non-combustible aerosol provision device 100 for generating aerosol from an aerosol generating medium/material such as the aerosol generating material 3 of the articles 1, 1′ described herein. In broad outline, the device 100 may be used to heat a replaceable article 110 comprising the aerosol generating medium, for instance the articles 1, 1′ described herein, to generate an aerosol or other inhalable medium which is inhaled by a user of the device 100. The device 100 and replaceable article 110 together form a system.

The device 100 comprises a housing 102 (in the form of an outer cover) which surrounds and houses various components of the device 100. The device 100 has an opening 104 in one end, through which the article 110 may be inserted for heating by a heating assembly. In use, the article 110 may be fully or partially inserted into the heating assembly where it may be heated by one or more components of the heater assembly.

The device 100 of this example comprises a first end member 106 which comprises a lid 108 which is moveable relative to the first end member 106 to close the opening 104 when no article 110 is in place. In FIG. 6, the lid 108 is shown in an open configuration, however the lid 108 may move into a closed configuration. For example, a user may cause the lid 108 to slide in the direction of arrow “B”.

The device 100 may also include a user-operable control element 112, such as a button or switch, which operates the device 100 when pressed. For example, a user may turn on the device 100 by operating the switch 112.

The device 100 may also comprise an electrical component, such as a socket/port 114, which can receive a cable to charge a battery of the device 100. For example, the socket 114 may be a charging port, such as a USB charging port.

FIG. 7 depicts the device 100 of FIG. 6 with the outer cover 102 removed and without an article 110 present. The device 100 defines a longitudinal axis 134.

As shown in FIG. 7, the first end member 106 is arranged at one end of the device 100 and a second end member 116 is arranged at an opposite end of the device 100. The first and second end members 106, 116 together at least partially define end surfaces of the device 100. For example, the bottom surface of the second end member 116 at least partially defines a bottom surface of the device 100. Edges of the outer cover 102 may also define a portion of the end surfaces. In this example, the lid 108 also defines a portion of a top surface of the device 100.

The end of the device closest to the opening 104 may be known as the proximal end (or mouth end) of the device 100 because, in use, it is closest to the mouth of the user. In use, a user inserts an article 110 into the opening 104, operates the user control 112 to begin heating the aerosol generating material and draws on the aerosol generated in the device. This causes the aerosol to flow through the device 100 along a flow path towards the proximal end of the device 100.

The other end of the device furthest away from the opening 104 may be known as the distal end of the device 100 because, in use, it is the end furthest away from the mouth of the user. As a user draws on the aerosol generated in the device, the aerosol flows away from the distal end of the device 100.

The device 100 further comprises a power source 118. The power source 118 may be, for example, a battery, such as a rechargeable battery or a non-rechargeable battery. Examples of suitable batteries include, for example, a lithium battery (such as a lithium-ion battery), a nickel battery (such as a nickel-cadmium battery), and an alkaline battery. The battery is electrically coupled to the heating assembly to supply electrical power when required and under control of a controller (not shown) to heat the aerosol generating material. In this example, the battery is connected to a central support 120 which holds the battery 118 in place.

The device further comprises at least one electronics module 122. The electronics module 122 may comprise, for example, a printed circuit board (PCB). The PCB 122 may support at least one controller, such as a processor, and memory. The PCB 122 may also comprise one or more electrical tracks to electrically connect together various electronic components of the device 100. For example, the battery terminals may be electrically connected to the PCB 122 so that power can be distributed throughout the device 100. The socket 114 may also be electrically coupled to the battery via the electrical tracks.

In the example device 1X), the heating assembly is an inductive heating assembly and comprises various components to heat the aerosol generating material of the article 110 via an inductive heating process. Induction heating is a process of heating an electrically conducting object (such as a susceptor) by electromagnetic induction. An induction heating assembly may comprise an inductive element, for example, one or more inductor coils, and a device for passing a varying electric current, such as an alternating electric current, through the inductive element. The varying electric current in the inductive element produces a varying magnetic field. The varying magnetic field penetrates a susceptor suitably positioned with respect to the inductive element, and generates eddy currents inside the susceptor. The susceptor has electrical resistance to the eddy currents, and hence the flow of the eddy currents against this resistance causes the susceptor to be heated by Joule heating. In cases where the susceptor comprises ferromagnetic material such as iron, nickel or cobalt, heat may also be generated by magnetic hysteresis losses in the susceptor, i.e. by the varying orientation of magnetic dipoles in the magnetic material as a result of their alignment with the varying magnetic field. In inductive heating, as compared to heating by conduction for example, heat is generated inside the susceptor, allowing for rapid heating. Further, there need not be any physical contact between the inductive heater and the susceptor, allowing for enhanced freedom in construction and application.

The induction heating assembly of the example device 100 comprises a susceptor arrangement 132 (herein referred to as “a susceptor”), a first inductor coil 124 and a second inductor coil 126. The first and second inductor coils 124, 126 are made from an electrically conducting material. In this example, the first and second inductor coils 124, 126 are made from Litz wire/cable which is wound in a helical fashion to provide helical inductor coils 124, 126. Litz wire comprises a plurality of individual wires which are individually insulated and are twisted together to form a single wire. Litz wires are designed to reduce the skin effect losses in a conductor. In the example device 100, the first and second inductor coils 124, 126 are made from copper Litz wire which has a rectangular cross section. In other examples the Litz wire can have other shape cross sections, such as circular.

The first inductor coil 124 is configured to generate a first varying magnetic field for heating a first section of the susceptor 132 and the second inductor coil 126 is configured to generate a second varying magnetic field for heating a second section of the susceptor 132. In this example, the first inductor coil 124 is adjacent to the second inductor coil 126 in a direction along the longitudinal axis 134 of the device 100 (that is, the first and second inductor coils 124, 126 to not overlap). The susceptor arrangement 132 may comprise a single susceptor, or two or more separate susceptors. Ends 130 of the first and second inductor coils 124, 126 can be connected to the PCB 122.

It will be appreciated that the first and second inductor coils 124, 126, in some examples, may have at least one characteristic different from each other. For example, the first inductor coil 124 may have at least one characteristic different from the second inductor coil 126. More specifically, in one example, the first inductor coil 124 may have a different value of inductance than the second inductor coil 126. In FIG. 2, the first and second inductor coils 124, 126 are of different lengths such that the first inductor coil 124 is wound over a smaller section of the susceptor 132 than the second inductor coil 126. Thus, the first inductor coil 124 may comprise a different number of turns than the second inductor coil 126 (assuming that the spacing between individual turns is substantially the same). In yet another example, the first inductor coil 124 may be made from a different material to the second inductor coil 126. In some examples, the first and second inductor coils 124, 126 may be substantially identical.

In this example, the first inductor coil 124 and the second inductor coil 126 are wound in opposite directions. This can be useful when the inductor coils are active at different times. For example, initially, the first inductor coil 124 may be operating to heat a first section/portion of the article 110, and at a later time, the second inductor coil 126 may be operating to heat a second section/portion of the article 110. Winding the coils in opposite directions helps reduce the current induced in the inactive coil when used in conjunction with a particular type of control circuit. In FIG. 7 the device 100, the first inductor coil 124 is a right-hand helix and the second inductor coil 126 is a left-hand helix. However, in another embodiment, the inductor coils 124, 126 may be wound in the same direction, or the first inductor coil 124 may be a left-hand helix and the second inductor coil 126 may be a right-hand helix.

The susceptor 132 of this example is hollow and therefore defines a receptacle within which aerosol generating material is received. For example, the article 110 can be inserted into the susceptor 132. In this example the susceptor 120 is tubular, with a circular cross section.

The susceptor 132 may be made from one or more materials. Preferably the susceptor 132 comprises carbon steel having a coating of Nickel or Cobalt.

In some examples, the susceptor 132 may comprise at least two materials capable of being heated at two different frequencies for selective aerosolization of the at least two materials. For example, a first section of the susceptor 132 (which is heated by the first inductor coil 124) may comprise a first material, and a second section of the susceptor 132 which is heated by the second inductor coil 126 may comprise a second, different material. In another example, the first section may comprise first and second materials, where the first and second materials can be heated differently based upon operation of the first inductor coil 124. The first and second materials may be adjacent along an axis defined by the susceptor 132, or may form different layers within the susceptor 132. Similarly, the second section may comprise third and fourth materials, where the third and fourth materials can be heated differently based upon operation of the second inductor coil 126. The third and fourth materials may be adjacent along an axis defined by the susceptor 132, or may form different layers within the susceptor 132. Third material may the same as the first material, and the fourth material may be the same as the second material, for example. Alternatively, each of the materials may be different. The susceptor may comprise carbon steel or aluminum for example.

The device 100 of FIG. 7 further comprises an insulating member 128 which may be generally tubular and at least partially surround the susceptor 132. The insulating member 128 may be constructed from any insulating material, such as plastic for example. In this particular example, the insulating member is constructed from polyether ether ketone (PEEK). The insulating member 128 may help insulate the various components of the device 100 from the heat generated in the susceptor 132.

The insulating member 128 can also fully or partially support the first and second inductor coils 124, 126. For example, as shown in FIG. 7, the first and second inductor coils 124, 126 are positioned around the insulating member 128 and are in contact with a radially outward surface of the insulating member 128. In some examples the insulating member 128 does not abut the first and second inductor coils 124, 126. For example, a small gap may be present between the outer surface of the insulating member 128 and the inner surface of the first and second inductor coils 124, 126.

In a specific example, the susceptor 132, the insulating member 128, and the first and second inductor coils 124, 126 are coaxial around a central longitudinal axis of the susceptor 132.

FIG. 8 shows a side view of device 100 in partial cross-section. The outer cover 102 is present in this example. The rectangular cross-sectional shape of the first and second inductor coils 124, 126 is more clearly visible.

The device 100 further comprises a support 136 which engages one end of the susceptor 132 to hold the susceptor 132 in place. The support 136 is connected to the second end member 116.

The device may also comprise a second printed circuit board 138 associated within the control element 112.

The device 100 further comprises a second lid/cap 140 and a spring 142, arranged towards the distal end of the device 100. The spring 142 allows the second lid 140 to be opened, to provide access to the susceptor 132. A user may open the second lid 140 to clean the susceptor 132 and/or the support 136.

The device 100 further comprises an expansion chamber 144 which extends away from a proximal end of the susceptor 132 towards the opening 104 of the device. Located at least partially within the expansion chamber 144 is a retention clip 146 to abut and hold the article 110 when received within the device 1M. The expansion chamber 144 is connected to the end member 106.

FIG. 9 is an exploded view of the device 100 of FIG. 8, with the outer cover 102 omitted.

FIG. 10A depicts a cross section of a portion of the device 100 of FIG. 8. FIG. 10B depicts a close-up of a region of FIG. 10A. FIGS. 10A and 10B show the article 110 received within the susceptor 132, where the article 110 is dimensioned so that the outer surface of the article 110 abuts the inner surface of the susceptor 132. This ensures that the heating is most efficient. The article 110 of this example comprises aerosol generating material 110 a. The aerosol generating material 110 a is positioned within the susceptor 132. The article 110 may also comprise other components such as a filter, wrapping materials and/or a cooling structure.

FIG. 10B shows that the outer surface of the susceptor 132 is spaced apart from the inner surface of the inductor coils 124, 126 by a distance 150, measured in a direction perpendicular to a longitudinal axis 158 of the susceptor 132. In one particular example, the distance 150 is about 3 mm to 4 mm, about 3-3.5 mm, or about 3.25 mm.

FIG. 10B further shows that the outer surface of the insulating member 128 is spaced apart from the inner surface of the inductor coils 124, 126 by a distance 152, measured in a direction perpendicular to a longitudinal axis 158 of the susceptor 132. In one particular example, the distance 152 is about 0.05 mm. In another example, the distance 152 is substantially 0 mm, such that the inductor coils 124, 126 abut and touch the insulating member 128.

In one example, the susceptor 132 has a wall thickness 154 of about 0.025 mm to 1 mm, or about 0.05 mm.

In one example, the susceptor 132 has a length of about 40 mm to 60 mm, about 40 mm to 45 mm, or about 44.5 mm.

In one example, the insulating member 128 has a wall thickness 156 of about 0.25 mm to 2 mm, 0.25 mm to 1 mm, or about 0.5 mm.

In use, the articles 1, 1′ described herein can be inserted into a non-combustible aerosol provision device such as the device 100 described with reference to FIGS. 6 to 10. At least a portion of the mouthpiece 2, 2′ of the article 1, 1′ protrudes from the non-combustible aerosol provision device 100 and can be placed into a user's mouth. An aerosol is produced by heating the aerosol generating material 3 using the device 100. The aerosol produced by the aerosol generating material 3 passes through the mouthpiece 2 to the user's mouth.

The articles 1, 1′ described herein have particular advantages, for instance when used with non-combustible aerosol provision devices such as the device 100 described with reference to FIGS. 6 to 10. In particular, the first tubular element 4 formed from filamentary tow has surprisingly been found to have a significant influence on the temperature of the outer surface of the mouthpiece 2, 2′ of the articles 1, 1′. For instance, where the hollow tubular element 4 formed from filamentary tow is wrapped in an outer wrapper, for instance the tipping paper 5, an outer surface of the outer wrapper has been found to reach a maximum temperature of less than 42° C. during use, suitably less than 40° C. and more suitably less than 38° C. or less than 36° C.

The various embodiments described herein are presented only to assist in understanding and teaching the claimed features. These embodiments are provided as a representative sample of embodiments only, and are not exhaustive and/or exclusive. It is to be understood that advantages, embodiments, examples, functions, features, structures, and/or other aspects described herein are not to be considered limitations on the scope of the invention as defined by the claims or limitations on equivalents to the claims, and that other embodiments may be utilised and modifications may be made without departing from the scope of the claimed invention. Various embodiments of the invention may suitably comprise, consist of, or consist essentially of, appropriate combinations of the disclosed elements, components, features, parts, steps, means, etc, other than those specifically described herein. In addition, this disclosure may include other inventions not presently claimed, but which may be claimed in future.

EXAMPLES Experimental Determination of Nicotine and Aerosol Forming Material Content

The quantities of nicotine and the aerosol forming material may be measured using the following method.

An extraction solution may be made as follows. 2.5±0.01 g of n-heptadecane is weighed into a weighing vessel and added to a 5 L volumetric flask, containing 400-500 mL of methanol and the contents of the volumetric flask thoroughly mixed to dissolve the n-heptadecane. When dissolved, methanol is added to make up to the correct volume of the volumetric flask and form the extraction solution.

The aerosol generating material (5-10 mm wide pieces) is stored in a sealed plastic bag or air tight container before analysis. The samples are mixed inside the bags before use, as to guarantee homogeneity.

1.0 g (±0.01 g) of the sample is weighed into a 150-mL conical flask. 1.00 mL of deionized water from a calibrated pipette is added and the mixture left for 5 minutes. 50 mL of the extraction solution (see above) is added with a calibrated dispenser. The flask is stoppered and then set shaking on an Orbital/Horizontal shaker for 3 hours at 150 rpm.

Using a plastic 5 mL syringe, some of the extract is filtered through a 0.45 μm PVDF filter into a 2 mL GC Vial.

The extract in the GC vial may then be analyzed using GC (see below tables for parameters) against working calibration solutions that have been previously prepared.

The sample is injected into the injection port connected to the analytical column. A capillary GC column (phenomenex ZB-WAXplus (30 m×0.53 mm id×1.00 μm)) and a flame ionization detector (FID) may be used for the analysis.

TABLE 1 Column Parameters Front - MNPH Column ZB-WAXplus 30 m × 0.53 mm × 1.00 μm Carrier Gas Helium Pressure (psi) 5.1

TABLE 2 Inlet/Injector Parameters Front - MNPH Mode Splitless Temperature (° C.) 270 Pressure (psi) 5.1 Split Ratio N/A Split Flow (mL/min) N/A Total Flow (mL/min) 48 Injection Volume (μL) 1 Gas Saver On

TABLE 3 Detector Parameters Front - MNPH Type FID Temperature (° C.) 270 H₂ Flow/Ref. Flow 30 Air Flow (mL/min) 400 Make Up Constant Make Up He (mL/min) 15.0 On/Off Flame On Negative Polarity N/A

TABLE 4 Oven Parameters Initial Temperature 120° C. Initial Time 4 min Ramp Rate 20° C./min Final Temperature 230° C. Final Time 2.5 min

The final results of nicotine and aerosol forming material [CNH (%) (dwb)] may be expressed as percent of dried sample, corrected by water content using the below equations. Water content may be determined by the Karl Fisher Method.

${C_{NH}\left( \frac{mg}{g} \right)} = \frac{\left( {\frac{A_{NH}}{A_{ISTD}} - {INT}} \right) \times C_{ISTD} \times V}{D \times m}$ ${{C_{NH}(\%)}\mspace{14mu}({dwb})} = {\frac{{C_{NH}\left( \frac{mg}{g} \right)} \times 100}{1000} \times \frac{100}{100 - C_{{Water}\mspace{14mu}{(\%)}}}}$

NH: Nicotine and/or Humectants (propylene glycol and glycerol) analytes CNH (mg g): Concentration of the Analyte expressed in mg/g CNH (%) (dwb): Concentration of the Analyte expressed in % of dried sample Dwb: dry weigh bases CWater (%): Concentration of Water expressed in % ANH: Area of the analyte (nicotine, glycerol or propylene glycol) AISTD: Area of the internal standard INT: y-axis intercept of the linear regression CISTD: concentration of internal standard in the extraction solution (mg/mL) V: volume of extraction solution (mL)+1.00 mL of deionized water D: slope ofthe linear regression m: mass of whole THP recon used for extraction (g)

The nicotine target % provided herein may be determined by analyzing the nicotine content of a series of samples (e.g. 20-40 samples) and then taking an average.

Determination of Water Content

In the compositions described herein, the % by weight refers to a dry weight basis, unless specifically indicated to the contrary. Thus, any water that may be present in the tobacco composition, or in any component thereof, is entirely disregarded for the purposes of the determination of the weight %. However, other liquid components, such as the aerosol forming material, are included in the weight %. The water content of the tobacco compositions described herein may vary and may be, for example, from 5 to 15% by weight. The water content can be determined by Karl-Fisher analysis.

Water Content by Karl-Fisher Analysis

Karl Fisher water analysis may be performed on a Mettler Toledo Karl Fisher V30 Volumetric Titrator. Prior to sample testing the background water content of the extraction solvent (methanol) is determined and the value recorded in the analysis method.

Approximately 0.5 g of material to be analyzed is accurately weighed (4 decimal places) into a 100 mL conical flask and the weight recorded. 50 mL of dry methanol is dispensed into the conical flask which is then sealed and agitated on a flatbed shaker (155 rpm) for 30 minutes. Approximately 2 mL of the sample extract is taken up in a syringe and injected into the titration apparatus (weight determined by back weighing of syringe). Results are reported as the % water content of the sample by weight. Samples are determined in triplicate and the averaged values reported along with the standard deviation.

Leaf Material

Nine blends consisting of leaf material were prepared. The amount of nicotine in each blend by weight of the blend can be determined. The results are shown in Tables 5 and 5a:

TABLE 5 Blends of Leaf Material Inclusion Inclusion Nicotine (KG) (%) (%) Virginia Leaf Virginia 400  10% 2.57 Virginia 200   5% 3.04 Virginia 200   5% 3.52 800  20% 2.92 Oriental safe Virginia 200 6.8% 2.57 Oriental 210 7.1% 0.95 Oriental 140 4.7% 1.24 550 18.6%  1.61 Dark flue-cured (DFC) safe Virginia 200 6.9% 2.57 Oriental 210 7.2% 0.95 Fired Cured 100 3.4% 3.04 510 17.5%  1.99 Dark flue-cured (DFC) stretch Virginia 200 6.6% 2.57 Oriental 210 7.0% 0.95 Fired Cured 200 6.6% 3.04 610 20.3%  2.16 Burley Leaf Burley 200 6.8% 2.95 Oriental 210 7.1% 0.95 Oriental 140 4.7% 1.43 550 18.6%  1.80 Dark Air-Cured (DAC) Virginia 200 6.6% 2.57 Oriental 210 7.0% 0.95 Dark Air Cured 210 7.0% 1.43 620 20.5%  1.63

TABLE 5a Blends of Leaf Material Inclusion (KG) Inclusion (%) Nicotine (%) Virginia Leaf A Virginia 1 400 12.8 2.57 Virginia 2 200 6.4 2.57 Virginia 3 400 12.8 2.57 Virginia 4 200 6.4 3.04 1200 38.5 2.64 Burley Leaf A Virginia 5 200 6.6 3.52 Burley 1 200 6.6 2.95 Burley 2 200 6.6 2.95 Oriental 1 210 7.0 0.95 Oriental 2 140 4.7 1.24 Oriental 3 140 4.7 1.43 1090 36.2 2.25 Virginia Leaf B Virginia 1 400 13.0 2.09 Virginia 6 400 13.0 2.57 Virginia 2 200 6.5 2.57 Virginia 3 400 13.0 2.57 Virginia 4 400 13.0 3.04 1800 58.4 2.57

Comparative Examples

Six tobacco reconstituted tobacco materials (Recon. Tobacco 1-6) comprising Low Nicotine Reconstituted Tobacco (LNRT) and/or Medium Nicotine Reconstituted Tobacco (MNRT) and/or High Nicotine Reconstituted Tobacco (HNRT) were prepared and then analyzed to ascertain their nicotine content. The results are shown in Table 6 and Table 6a.

TABLE 6 Reconstituted Tobacco Materials Components of Reconstituted Recon. Recon. Recon. Tobacco Material Tobacco 1 Tobacco 2 Tobacco 3 LNRT 77.0 38.4 0.0 MNRT 0.0 0.0 0.0 HNRT 0.0 38.4 76.5 Virginia leaf 0.0 0.0 0.0 Burley leaf 0.0 0.0 0.0 Oriental leaf 0.0 0.0 0.0 Tobacco total 77.0 76.8 76.5 Wood pulp 8.0 8.3 8.5 Glycerol in Recon 15.0 15.0 15.0 Glycerol added (%) 0.0 0.0 0.0 Grand total 100.0 100.0 100.0 Nicotine Target % 0.85 1.18 1.50 Glycerol added (%) 0.00 0.00 0.00 Cuts per inch (CPI) 22 22 22 Rod Net weight (mg) 260 260 260

It will be noted that the nicotine content of the reconstituted tobacco materials was less than or equal to 1.5% by weight.

TABLE 6a Reconstituted Tobacco Materials Components of Reconstituted Recon. Recon. Recon. Tobacco Material Tobacco 4 Tobacco 5 Tobacco 6 LNRT 77.0 0.0 0.0 MNRT 0.0 77.0 0.0 HNRT 0.0 0.0 76.5 Virginia leaf 0.0 0.0 0.0 Burley leaf 0.0 0.0 0.0 Oriental leaf 0.0 0.0 0.0 Tobacco total 77.0 77.0 76.5 Wood pulp 8.0 8.0 8.5 Glycerol in Recon 15.0 15.0 15.0 Glycerol added (%) 0.0 0.0 0.0 Grand total 100.0 100.0 100.0 Nicotine Target % 1.15 1.30 1.50 Glycerol added (%) 0.00 0.00 0.00 Cuts per inch (CPI) 32 32 37 Rod Net weight (mg)* 260 260 260 *rods having a net weight of 340 mg were also made

It will be noted that the nicotine content of the reconstituted tobacco materials as less than or equal to 1.5% by weight.

Examples 1-3

Three blends comprising leaf tobacco. Low Nicotine Reconstituted Tobacco (LNRT) and/or Medium Nicotine Reconstituted Tobacco (MNRT) and/or High Nicotine Reconstituted Tobacco (HNRT) were prepared and then analyzed for their nicotine content. The results are shown in Table 7.

TABLE 7 Example Blends 1-3 Components Blend 1 Blend 2 Blend 3 Virginia grade/LNRC 61.6 30.7 0.0 Virginia grade/MNRC 0.0 0.0 0.0 Virginia grade/HNRC 0.0 30.7 61.2 Virginia grade/Lamina 18.0 18.0 18.0 Burley grade 0.0 0.0 0.0 Oriental grade 0.0 0.0 0.0 Tobacco total 79.6 79.4 79.2 Wood pulp 6.4 6.6 6.8 Glycerol in Recon 12.0 12.0 12.0 Glycerol added (%) 2.0 2.0 2.0 Grand total 100.0 100.0 100.0 Nicotine Target % 1.25 1.50 1.75 Cuts per Inch (CPI) 22 22 22 Rod Net weight (mg) 260 260 260

Examples 4-21

18 further blends comprising leaf tobacco and reconstituted tobacco material were prepared and then analyzed for their nicotine content. The results are shown in Tables 8, 9, 9a, 9b and 9c.

TABLE 8 Example Blends 4-8 Components of Recon Blend 4 Blend 5 Blend 6 Blend 7 Blend 8 Virginia grade/ 62.7 31.2 63.5 31.7 61.4 LNRC Virginia grade/ 0.0 0.0 0.0 0.0 0.0 MNRC Virginia grade/ 0.0 31.2 0.0 31.7 0.0 HNRC Virginia grade/Leaf 6.1 6.1 6.2 6.2 6.0 Burley grade/Leaf 0.0 0.0 0.0 0.0 0.0 Oriental grade/Leaf 10.6 10.6 6.5 6.5 6.3 DAC grade/Leaf 0.0 0.0 0.0 0.0 0.0 DFC grade/Leaf 0.0 0.0 3.1 3.1 6.0 Tobacco total 79.4 79.2 79.3 79.1 79.6 Wood pulp 6.5 6.7 6.6 6.8 6.4 Glycerol in Recon 12.1 12.1 12.1 12.1 12.0 Glycerol added (%) 2.0 2.0 2.0 2.0 2.0 Grand total 100.0 100.0 100.0 100.0 100.0 Nicotine Target (%) 1.00 1.25 1.05 1.30 1.15 Cuts per Inch (CPI) 22 22 22 22 22 Rod Net weight (mg) 260 260 260 260 260

TABLE 9 Example Blends 9-13 Blend Blend Blend Blend Components of Recon Blend 9 10 11 12 13 Virginia grade/LNRC 30.6 62.7 31.2 61.2 30.5 Virginia grade/ 0.0 0.0 0.0 0.0 0.0 MNRC Virginia grade/HNRC 30.6 0.0 31.2 0.0 30.5 Virginia grade/Leaf 6.0 0.0 0.0 5.9 5.9 Burley grade/Leaf 0.0 6.1 6.1 0.0 0.0 Oriental grade/Leaf 6.3 10.7 10.7 6.2 6.2 DAC grade/Leaf 0.0 0.0 0.0 6.2 6.2 DFC grade/Leaf 6.0 0.0 0.0 0.0 0.0 Tobacco total 79.4 79.4 79.2 79.6 79.4 Wood pulp 6.6 6.5 6.7 6.4 6.6 Glycerol in Recon 12.0 12.1 12.1 12.0 12.0 Glycerol added (%) 2.0 2.0 2.0 2.0 2.0 Grand total 100.0 100.0 100.0 100.0 100.0 Nicotine Target % 1.40 1.05 1.30 1.15 1.40 Cuts per Inch (CPI) 22 22 22 22 22 Rod Net weight (mg) 260 260 260 260 260

TABLE 9a Example Blends 14-15 Components of Recon Blend 14 Blend 15 Virginia grade/LNRC (%) 0.0 0.0 Virginia grade/MNRC (%) 0.0 60.4 Virginia grade/HNRC (%) 60.0 0.0 Virginia grade/Leaf (%) 19.5 19.6 Burley grade/Leaf (%) 0.0 0.0 Oriental grade/Leaf (%) 0.0 0.0 DAC grade/Leaf (%) 0.0 0.0 DFC grade/Leaf (%) 0.0 0.0 Tobacco total (%) 79.5 80.0 Wood pulp (%) 6.2 6.3 Glycerol in Recon (%) 11.7 11.8 Glycerol added (%) 2.0 2.0 Casings added (%) 0.6 0 Grand total (%) 100 100 Nicotine Target (%) 1.75 1.60 Cuts per Inch (CPI) 22 32 Rod Net weight (mg)* 260 260 *rods having a net weight of 340 mg were also made

TABLE 9b Example Blends 16-18 Components of Recon Blend 16 Blend 17 Blend 18 Virginia grade/LNRC (%) 0.0 44.1 0.0 Virginia grade/MNRC (%) 0.0 0.0 44.1 Virginia grade/HNRC (%) 44.2 0.0 0.0 Virginia grade/Leaf A (%) 36.1 36.0 36.0 Burley grade/Leaf A (%) 0.0 0.0 0.0 Oriental grade/Leaf (%) 0.0 0.0 0.0 DAC grade/Leaf (%) 0.0 0.0 0.0 DFC grade/Leaf (%) 0.0 0.0 0.0 Tobacco total (%) 80.3 80.1 80.1 Wood pulp (%) 4.9 4.9 4.9 Glycerol in Recon (%) 8.7 8.6 8.6 Glycerol added (%) 5.6 5.6 5.6 Casings added (%) 0.5 0.8 0.8 Grand total (%) 100 100 100 Nicotine Target (%) 1.80 1.60 1.15 Cuts per Inch (CPI) 32 22 32 Rod Net weight (mg)* 260 260 260 *rods having a net weight of 340 mg were also made

TABLE 9c Example Blends 19-21 Components of Recon Blend 19 Blend 20 Blend 21 Virginia grade/LNRC (%) 0.0 0.0 29.2 Virginia grade/MNRC (%) 0.0 29.2 0.0 Virginia grade/HNRC (%) 29.2 0.0 0.0 Virginia grade/Leaf B (%) 53.7 53.7 53.7 Burley grade/Leaf (%) 0.0 0.0 0.0 Oriental grade/Leaf (%) 0.0 0.0 0.0 DAC grade/Leaf (%) 0.0 0.0 0.0 DFC grade/Leaf (%) 0.0 0.0 0.0 Tobacco total (%) 82.9 82.9 82.9 Wood pulp (%) 3.2 3.2 3.2 Glycerol in Recon (%) 5.7 5.7 5.7 Glycerol added (%) 7.4 7.4 7.4 Casings added (%) 0.8 0.8 0.8 Grand total (%) 100 100 100 Nicotine Target (%) 1.95 1.85 1.75 Cuts per Inch (CPI) 32 32 32 Rod Net weight (mg)* 260 260 260 *rods having a net weight of 340 mg were also made

The results show that the nicotine content of tobacco compositions can be tailored by combining the reconstituted tobacco material with leaf tobacco having a nicotine content of greater than about 1.5% by weight of the leaf tobacco. Thus, a variety of tobacco compositions having a broad range of nicotine concentrations can be manufactured.

Table 10 below shows the temperature of the outer surface of the article 1 as descrnbed with reference to FIG. 4 herein when heated using the device 100 described with reference to FIGS. 6 to 10B herein. First, second and third temperature measuring probes were used as corresponding first, second and third positions along the mouthpiece 2 of the article 1. The first position (numbered as position 1 in Table 10) was at 4 mm from the downstream end 2 b of the mouthpiece 2, the second position (numbered as position 2 in Table 10) was at 8 mm from the downstream end 2 b of the mouthpiece 2, and the third position (numbered as position 3 in Table 10) was at 12 mm from the downstream end 2 b of the mouthpiece 2.

The first position was therefore on the outer surface of the part of the mouthpiece 2 in which the first tubular element 4 is disposed, while the second and third positions were on the outer surface of the part of the mouthpiece 2 in which the body of material 6 is disposed.

A control article was tested for comparison with the filamentary tow tubular elements 4 described herein, and used instead of the filamentary tow tubular element 4 a known spirally wrapped paper tube having the same construction as the second hollow tubular element 8 described herein, but a length of 6 mm rather than 25 mm.

Testing was performed for the first 5 puffs on the article, since by the 5^(th) puff temperatures have generally peaked and are starting to fall, so that an approximate maximum temperature can be observed. Each sample was tested 5 times, and the temperatures provided are an average of these 5 tests. The known Health Canada Intense puffing regime was applied (55 ml puff volume applied for 2 seconds duration every 30 seconds) using standard testing equipment.

As shown in the table below, surprisingly, it was found that the use of a tubular element 4 formed from filamentary tow reduced the outer surface temperature of the mouthpiece 2 as compared to the control article in every puff and at every testing position on the mouthpiece 2. The tubular element 4 formed from filamentary tow was particular effective at reducing the temperature at the first probe position, where consumer's lips will be positioned when using the article 1. In particular, the temperature of the outer surface of the mouthpiece 2 at the first probe position was reduced by more than 7° C. in the first three puffs and by more than 5° C. in the fourth and fifth puffs.

TABLE 10 Temperature (° C.) of the Outer Article Surface Probe Consumable Pos. Mouth End Puff 1 Puff 2 Puff 3 Puff 4 Puff 5 1 Paper Tube 38.98 42.50 43.26 42.38 40.52 (control) Tow tubular 31.79 35.00 35.72 35.46 34.64 element 4 2 Paper Tube 41.60 45.34 47.05 46.36 44.58 (control) Tow Tubular 40.32 43.48 43.73 43.21 41.73 element 4 3 Paper Tube 46.71 48.93 50.51 53.14 54.63 (control) Tow Tubular 45.43 47.73 47.64 47.72 47.36 element 4

FIG. 11 illustrates a method of manufacturing an article for use in a non-combustible aerosol provision system. At step S101, first and second portions of aerosol generating material, each comprising an aerosol forming material, are positioned adjacent to respective first and second longitudinal ends of a mouthpiece rod, the mouthpiece rod comprising a hollow tubular element rod formed from filamentary tow disposed between the first and second ends. In the present example, the hollow tubular element rod comprises a double length first hollow tubular element 4 arranged between first and second respective bodies of material 6. At the outer end of each body of material 6 is positioned a respective second tubular element 8 and it is adjacent to the outer ends of these second tubular elements B that the first and second portions of aerosol generating material are positioned. The mouthpiece rod is wrapped in the second plug wrap described herein.

At step S102, the first and second portions of aerosol generating material are connected to the mouthpiece rod. In the present example, this is performed by wrapping a tipping paper 5 as described herein around the mouthpiece rod and at least part of each of the portions of aerosol generating material 3. In the present example, the tipping paper 5 extends about 5 mm longitudinally over the outer surface of each of the portioned of aerosol generating material 3.

At step S103, the hollow tubular element rod is cut to form first and second articles, each article comprising a mouthpiece comprising a portion of the hollow tubular element rod at the downstream end of the mouthpiece. In the present example, double length first hollow tubular element 4 of the mouthpiece rod is cut at a position about half-way along its length, so as to form first and second substantially identical articles.

The various embodiments described herein are presented only to assist in understanding and teaching the claimed features. These embodiments are provided as a representative sample of embodiments only, and are not exhaustive and/or exclusive. It is to be understood that advantages, embodiments, examples, functions, features, structures, and/or other aspects described herein are not to be considered limitations on the scope of the invention as defined by the claims or limitations on equivalents to the claims, and that other embodiments may be utilized and modifications may be made without departing from the scope of the claimed invention. Various embodiments of the invention may suitably comprise, consist of, or consist essentially of, appropriate combinations of the disclosed elements, components, features, parts, steps, means, etc, other than those specifically described herein. In addition, this disclosure may include other inventions not presently claimed, but which may be claimed in future. 

1. A tobacco composition comprising a tobacco component and an aerosol forming material, wherein the tobacco component comprises leaf tobacco material in an amount of between about 10% and about 90% by weight of the tobacco component and wherein the leaf tobacco material has a nicotine content of greater than 1.5% by weight of the leaf tobacco material.
 2. A tobacco composition as claimed in claim 1, wherein the leaf tobacco material comprises the aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material.
 3. A tobacco composition as claimed in claim 1, wherein the leaf tobacco material comprises said aerosol forming material in an amount of up to about 10% by weight of the leaf tobacco material, and wherein the tobacco composition comprises said aerosol forming material in an amount between about 10% and about 30% by weight of the tobacco composition.
 4. A tobacco composition as claimed in claim 1, wherein the tobacco component comprises menthol in an amount of between about 3 mg and about 16 mg.
 5. A tobacco composition as claimed in claim 1, wherein the total amount of the aerosol forming material is between about 10% and about 20% by weight of the tobacco composition.
 6. A tobacco composition as claimed in claim 1, wherein the tobacco component comprises leaf tobacco material in an amount of between about 11% and about 48% by weight of the tobacco component.
 7. A tobacco composition as claimed in claim 1, wherein the tobacco component comprises leaf tobacco material in an amount of between about 15% and about 25% by weight of the tobacco component.
 8. A tobacco composition as claimed in claim 1, wherein the tobacco component has a nicotine content up to 1.75% by weight of the tobacco component.
 9. A tobacco composition as claimed in claim 1, wherein the leaf tobacco material has a nicotine content of more than about 1.5% and up to about 4% by weight of the leaf tobacco material.
 10. A tobacco composition as claimed in claim 1, wherein the aerosol forming material is selected from the group consisting of glycerol, sorbitol, propylene glycol, triethylene glycol, lactic acid, diacetin, triacetin, triethylene glycol diacetate, triethyl citrate, ethyl myristate, isopropyl myristate, methyl stearate, dimethyl dodecanedioate, dimethyl tetradecanedioate, and mixtures thereof.
 11. A tobacco composition as claimed in claim 10, wherein the aerosol forming material comprises glycerol.
 12. A tobacco composition as claimed in claim 1, wherein the tobacco component comprises paper reconstituted tobacco material.
 13. A tobacco composition as claimed in claim 12, wherein the paper reconstituted tobacco material comprises the aerosol forming material in an amount of between about 10% and about 20% by weight of the reconstituted tobacco material.
 14. A tobacco composition as claimed in claim 12, wherein the tobacco component comprises paper reconstituted tobacco material in an amount of between about 50% and about 90% by weight of the tobacco component.
 15. A tobacco composition as claimed in claim 1, wherein the tobacco component comprises tobacco material selected from the group consisting of extruded tobacco, bandcast tobacco, and mixtures thereof.
 16. A tobacco composition as claimed in claim 1, wherein the tobacco composition comprises a filler.
 17. A tobacco composition as claimed in claim 16, wherein the tobacco composition comprises between about 5% and about 10% of the filler.
 18. A tobacco composition as claimed in claim 1, wherein the leaf tobacco material and/or the paper reconstituted tobacco material comprises a width of between about 0.5 mm and about 2 mm.
 19. A method of manufacturing the tobacco composition as claimed in claim 1, the method comprising applying said aerosol forming material to said leaf tobacco material.
 20. A method as claimed in claim 19, wherein the method further comprises combining the leaf tobacco material with paper reconstitute tobacco material comprising aerosol forming material in an amount of between 10% and 20% by weight of the paper reconstitute tobacco material. 21-22. (canceled)
 23. An article for use in an aerosol provision system comprising the tobacco composition as claimed in claim
 1. 24-30. (canceled)
 31. A system comprising a tobacco composition as claimed in claim 1 and a device arranged to heat the tobacco composition and generate an aerosol from the tobacco composition.
 32. (canceled) 